FDA 510(k)

FISCH DRILL PUMP

K-Number: K822900 · 1982-11-08

Decision Date1982-11-08

Product Code

DecisionSubstantially Equivalent

Device Summary

FISCH DRILL PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Teknar, Inc.. It received FDA 510(k) clearance on 1982-11-08 under 510(k) number K822900. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FISCH DRILL PUMP?

FISCH DRILL PUMP is a medical device that received FDA 510(k) clearance on 1982-11-08. The listed applicant is Teknar, Inc.. The 510(k) number is K822900.

When did FISCH DRILL PUMP receive FDA 510(k) clearance?

FISCH DRILL PUMP received FDA 510(k) clearance on 1982-11-08, under 510(k) number K822900.

Who is the listed applicant for FISCH DRILL PUMP?

The FDA 510(k) record lists Teknar, Inc. as the applicant. This does not by itself establish the device manufacturer.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.