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FDA 510(k)

REMOTE VACUUM BOOSTER SYSTEM, 7600 SERIES

K-Number: K884103 · 1989-03-03

ApplicantBoehringer Laboratories
Decision Date1989-03-03
Product CodeGCX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

REMOTE VACUUM BOOSTER SYSTEM, 7600 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 1989-03-03 under 510(k) number K884103. The device is classified under product code GCX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REMOTE VACUUM BOOSTER SYSTEM, 7600 SERIES?

REMOTE VACUUM BOOSTER SYSTEM, 7600 SERIES is a medical device that received FDA 510(k) clearance on 1989-03-03. The listed applicant is Boehringer Laboratories. The 510(k) number is K884103.

When did REMOTE VACUUM BOOSTER SYSTEM, 7600 SERIES receive FDA 510(k) clearance?

REMOTE VACUUM BOOSTER SYSTEM, 7600 SERIES received FDA 510(k) clearance on 1989-03-03, under 510(k) number K884103.

Who is the listed applicant for REMOTE VACUUM BOOSTER SYSTEM, 7600 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 REMOTE VACUUM BOOSTER SYSTEM, 7600 SERIES?

The FDA product code for REMOTE VACUUM BOOSTER SYSTEM, 7600 SERIES is GCX.

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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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