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FDA 510(k)

FLUID COOLED BONE SAW BLADE, 6000 SERIES

K-Number: K924953 · 1993-01-21

ApplicantBoehringer Laboratories
Decision Date1993-01-21
Product CodeGFA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FLUID COOLED BONE SAW BLADE, 6000 SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Boehringer Laboratories. It received FDA 510(k) clearance on 1993-01-21 under 510(k) number K924953. The device is classified under product code GFA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLUID COOLED BONE SAW BLADE, 6000 SERIES?

FLUID COOLED BONE SAW BLADE, 6000 SERIES is a medical device that received FDA 510(k) clearance on 1993-01-21. The listed applicant is Boehringer Laboratories. The 510(k) number is K924953.

When did FLUID COOLED BONE SAW BLADE, 6000 SERIES receive FDA 510(k) clearance?

FLUID COOLED BONE SAW BLADE, 6000 SERIES received FDA 510(k) clearance on 1993-01-21, under 510(k) number K924953.

Who is the listed applicant for FLUID COOLED BONE SAW BLADE, 6000 SERIES?

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

What is the FDA product code for FLUID COOLED BONE SAW BLADE, 6000 SERIES?

The FDA product code for FLUID COOLED BONE SAW BLADE, 6000 SERIES is GFA.

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Related Devices (Code: GFA)

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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.

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