510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
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K822900Substantially Equivalent

Fisch Drill Pump

Teknar, Inc., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K822900 is the FDA 510(k) clearance record for FISCH DRILL PUMP, cleared for Teknar, Inc. on . FDA records list 18 510(k) clearances for Teknar, Inc., from to . As of , FDA records show no recalls naming K822900.

Clearance record

Decision date
Received
(40 days to decision)
Review panel
Unknown
Applicant
Teknar, Inc. 4221 Richmond Rd., NW, Walker MI
Third party review
No