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FDA 510(k)

OSCILLATING BONE SAW BLADE, 6200 SERIES

K-Number: K934390 · 1994-01-26

ApplicantBoehringer Laboratories
Decision Date1994-01-26
Product CodeGFA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

OSCILLATING BONE SAW BLADE, 6200 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 1994-01-26 under 510(k) number K934390. 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 OSCILLATING BONE SAW BLADE, 6200 SERIES?

OSCILLATING BONE SAW BLADE, 6200 SERIES is a medical device that received FDA 510(k) clearance on 1994-01-26. The listed applicant is Boehringer Laboratories. The 510(k) number is K934390.

When did OSCILLATING BONE SAW BLADE, 6200 SERIES receive FDA 510(k) clearance?

OSCILLATING BONE SAW BLADE, 6200 SERIES received FDA 510(k) clearance on 1994-01-26, under 510(k) number K934390.

Who is the listed applicant for OSCILLATING BONE SAW BLADE, 6200 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 OSCILLATING BONE SAW BLADE, 6200 SERIES?

The FDA product code for OSCILLATING BONE SAW BLADE, 6200 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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