Clement Clarke, Inc.
MD, US
Clement Clarke, Inc. appears in FDA device records in MD. FDA records list 10 510(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
- 10
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 10 510(k) clearances for Clement Clarke, Inc. between 1979 and 1996. The busiest year on record is 1996, with 2. The most recent is 1996, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1979 | 1 |
| 1984 | 1 |
| 1990 | 1 |
| 1991 | 1 |
| 1992 | 1 |
| 1993 | 1 |
| 1994 | 1 |
| 1995 | 1 |
| 1996 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K961512 | PERKINS HAND-HELD APPLANATION TONOMETER | HKY | Substantially Equivalent | |
| K952713 | MINI WRIGHT LR AFS | BZH | Substantially Equivalent | |
| K953965 | 904 SLIT LAMP | HJO | Substantially Equivalent | |
| K932258 | OPTICOM M600 | HPT | Substantially Equivalent | |
| K914126 | VMX MINI-LOG FLOWMETER | BZH | Substantially Equivalent | |
| K914896 | FRIEDMANN ANALYSER 3 | HOK | Substantially Equivalent | |
| K912397 | PROFESSIONAL INDIRECT OPHTHALMOSCOPE | HLI | Substantially Equivalent | |
| K895953 | WRIGHT VENTILOMETER VM-1 | BZG | Substantially Equivalent | |
| K841430 | LASERSPEC | Substantially Equivalent | ||
| K781313 | VISION-STIMULATOR, CAM | HPL | 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
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain