Data / Medical devices / Malaysia / Meditop Corporation (M) Sdn Bhd
Meditop Corporation (M) Sdn Bhd: FDA-registered device maker in Baru Bangi,Selangor Darul Ehsa, Malaysia, 3 510(k) clearances
Meditop Corporation (M) Sdn Bhd is registered with the FDA (registration 1000587249) in Baru Bangi,Selangor Darul Ehsa, Malaysia. It lists 2 device types. The FDA files 3 510(k) clearances under its listings, the newest dated September 19, 1984. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1000587249
- Address
- Lot 1 Jalan P/1B, Kawasan Perindustrian Bangi, Bandar, Baru Bangi,Selangor Darul Ehsa, Malaysia, 43650
- Owner or operator
- TOP CORPORATION (8030272)
- Roles
- Manufacturer
- First device listed
- March 2, 2008
- Registered through
- 2026
- Brand names listed
- TOP DISPOSABLE INFUSION SET, TOP DISPOSABLE SPINAL NEEDLE, WINGED INFUSION SET
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Needle, Conduction, Anesthetic (W/Wo Introducer) | BSP | 2 | Manufacturer | accessdata.fda.gov |
| Set, Administration, Intravascular | FPA | 2 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| September 19, 1984 | K843313 | TOP DISPOSABLE SPINAL NEEDLE | BSP | Substantially Equivalent | Top Surgical Manufacturers Co. | accessdata.fda.gov |
| March 30, 1984 | K841025 | TOP DISPOSABLE INFUSION SET | FPA | Substantially Equivalent | Top Surgical Manufacturers Co. | accessdata.fda.gov |
| October 14, 1983 | K832622 | WINGED INFUSION SET | FPA | Substantially Equivalent | Top Surgical Manufacturers Co. | accessdata.fda.gov |
Compare with other makers
- All makers of Set, Administration, Intravascular
- All makers of Needle, Conduction, Anesthetic (W/Wo Introducer)
Updated September 19, 1984. 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.