Pymah Corp.
Somerville, NJ, US
Pymah Corp. appears in FDA device records in Somerville, NJ. FDA records list 11 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 11
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 11 510(k) clearances for Pymah Corp. between 1988 and 1995. The busiest year on record is 1993, with 3. The most recent is 1995, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1988 | 1 |
| 1989 | 2 |
| 1992 | 1 |
| 1993 | 3 |
| 1994 | 2 |
| 1995 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K934874 | STERIGAGE EO 100% | JOJ | Substantially Equivalent | |
| K943081 | TRIMLINE 2000 | DXN | Substantially Equivalent | |
| K925745 | ATI(R) DISP BIOLOGICAL-PLUS TEST PACK | FRC | Substantially Equivalent | |
| K925496 | ATI DISPOSABLE BIOLOGICAL-PLUS TEST PACK | FRC | Substantially Equivalent | |
| K924681 | GLUTARALDEHYDE MONITORS | JOJ | Substantially Equivalent | |
| K925744 | TEMPA-KUFF SINGLE PAT PRE-GAGED BALANCED DISP CUFF | DXQ | Substantially Equivalent | |
| K930604 | BALANCED(TM) NYLON BLADDER | DXQ | Substantially Equivalent | |
| K915170 | PYMAH COLD STERILOG GLUTARALDEHYDE MONITOR | MED | Substantially Equivalent | |
| K894399 | STERIGAGE INTEGRATOR TEST PACK FOR STEAM STERILI. | FRC | Substantially Equivalent | |
| K884421 | PRE-GAGED BALANCED CUFF W/SYLGARD ANTIMICRO. TREAT | DXQ | Substantially Equivalent | |
| K881286 | TEMPA-DOT CLINICAL THERMOMETER SHEATH | FQZ | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain