Data / Medical devices / United States / Aerospace Accessory Services Inc
Aerospace Accessory Services Inc: FDA-registered device maker in Medley, FL, United States, 2 510(k) clearances and 1 PMA approval
Aerospace Accessory Services Inc is registered with the FDA (registration 3006108746) in Medley, FL, United States. It lists 4 device types. The FDA files 2 510(k) clearances and 1 PMA approval under its listings, the newest dated January 12, 2017. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3006108746
- Address
- 10973 Nw 122nd St, Medley, FL, United States, 33178
- Owner or operator
- Aerospace Accessory Services Inc (10056228)
- Roles
- Repackager or relabeler
- First device listed
- November 20, 2017
- Registered through
- 2027
- Brand names listed
- 25D10055-2
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Automated External Defibrillators (Non-Wearable) | MKJ | 3 | Repackager or relabeler | accessdata.fda.gov |
| Emergency Response Safety Kit | OKI | 2 | Repackager or relabeler | accessdata.fda.gov |
| First Aid Kit Without Drug | OHO | 1 | Repackager or relabeler | accessdata.fda.gov |
| Over-The-Counter Automated External Defibrillator | NSA | 3 | Repackager or relabeler | 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 |
|---|---|---|---|---|---|---|
| February 25, 2005 | K050004 | PHILIPS HEARTSTART FRX DEFIBRILLATOR, MODEL 861304 | MKJ | Substantially Equivalent | Philips Medical Systems | accessdata.fda.gov |
| November 8, 2002 | K020715 | PHILIPS M5066A AND M5068A | MKJ | Substantially Equivalent - Subject to Tracking Reg. | Philips Medical Systems | accessdata.fda.gov |
PMA approvals
Premarket approvals this establishment lists, with the supplements the FDA has decided since.
| Approved | PMA number | Device | Product code | Supplements | Latest decision | Source |
|---|---|---|---|---|---|---|
| January 12, 2017 | P160008 | HeartSine Technologies LLC's samaritan Public Access Automated External Defibrillators (SAM 350P, SAM 360P and SAM 450P) | MKJ | 32 | June 22, 2026 | accessdata.fda.gov |
Compare with other makers
- All makers of First Aid Kit Without Drug
- All makers of Automated External Defibrillators (Non-Wearable)
- All makers of Over-The-Counter Automated External Defibrillator
- All makers of Emergency Response Safety Kit
Updated June 22, 2026. 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.