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FDA 510(k)

AUTOVAC BP SYSTE, 2000 SERIES

K-Number: K955010 · 1996-06-20

ApplicantBoehringer Laboratories
Decision Date1996-06-20
Product CodeCAC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AUTOVAC BP SYSTE, 2000 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 1996-06-20 under 510(k) number K955010. The device is classified under product code CAC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTOVAC BP SYSTE, 2000 SERIES?

AUTOVAC BP SYSTE, 2000 SERIES is a medical device that received FDA 510(k) clearance on 1996-06-20. The listed applicant is Boehringer Laboratories. The 510(k) number is K955010.

When did AUTOVAC BP SYSTE, 2000 SERIES receive FDA 510(k) clearance?

AUTOVAC BP SYSTE, 2000 SERIES received FDA 510(k) clearance on 1996-06-20, under 510(k) number K955010.

Who is the listed applicant for AUTOVAC BP SYSTE, 2000 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 AUTOVAC BP SYSTE, 2000 SERIES?

The FDA product code for AUTOVAC BP SYSTE, 2000 SERIES is CAC.

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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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