Data / Medical devices / United States / Rapid Aid Corp.
Rapid Aid Corp.: FDA-registered device maker in Wilmington, DE, United States, 3 510(k) clearances
Rapid Aid Corp. is registered with the FDA (registration 3010039589) in Wilmington, DE, United States. It lists 6 device types. The FDA files 3 510(k) clearances under its listings, the newest dated July 24, 2017. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3010039589
- Address
- 251 Little Falls Drive, Wilmington, DE, United States, 19808
- Owner or operator
- Rapid Aid Corp. (10028086)
- Roles
- Complaint file establishment
- First device listed
- December 29, 2008
- Registered through
- 2026
- Brand names listed
- 35059 Instant Cold Pack, Achilles Pack, Adhesive backed thermal skin patches, Ankle Pack, Calf/Shin Pack, Cold Pocket, Cold Slipper, Dorsum Pack and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessory, Surgical Apparel | LYU | 1 | Complaint file establishment | accessdata.fda.gov |
| Adhesive Backed Thermal Skin Patches | OMW | 1 | Complaint file establishment | accessdata.fda.gov |
| Bag, Ice | KYR | 1 | Complaint file establishment | accessdata.fda.gov |
| Infant Heel Warmer (Chemical Heat Pack) | MPO | 1 | Complaint file establishment | accessdata.fda.gov |
| Pack, Hot Or Cold, Disposable | IMD | 1 | Complaint file establishment | accessdata.fda.gov |
| Pack, Hot Or Cold, Reusable | IME | 1 | Complaint file establishment | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| July 24, 2017 | K163295 | Infant Transport Mattress Warmer with Disc | IMD | Substantially Equivalent | Rapid Aid Corp. | accessdata.fda.gov |
| May 27, 2015 | K150627 | Rapid Aid Instant Disposable Infant Heel Warmer | MPO | Substantially Equivalent | Rapid Aid Corp. | accessdata.fda.gov |
| May 3, 2004 | K040856 | RAPID AID INSTANT DISPOSABLE INFANT HEEL WARMER | MPO | Substantially Equivalent | Rapid Aid , Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Pack, Hot Or Cold, Reusable
- All makers of Pack, Hot Or Cold, Disposable
- All makers of Bag, Ice
- All makers of Infant Heel Warmer (Chemical Heat Pack)
- All makers of Adhesive Backed Thermal Skin Patches
- All makers of Accessory, Surgical Apparel
Updated July 24, 2017. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.