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FDA 510(k)

SUCTION REGULATOR 7700 SERIES

K-Number: K850200 · 1985-03-04

ApplicantBoehringer Laboratories
Decision Date1985-03-04
Product CodeKDP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SUCTION REGULATOR 7700 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 1985-03-04 under 510(k) number K850200. The device is classified under product code KDP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUCTION REGULATOR 7700 SERIES?

SUCTION REGULATOR 7700 SERIES is a medical device that received FDA 510(k) clearance on 1985-03-04. The listed applicant is Boehringer Laboratories. The 510(k) number is K850200.

When did SUCTION REGULATOR 7700 SERIES receive FDA 510(k) clearance?

SUCTION REGULATOR 7700 SERIES received FDA 510(k) clearance on 1985-03-04, under 510(k) number K850200.

Who is the listed applicant for SUCTION REGULATOR 7700 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 SUCTION REGULATOR 7700 SERIES?

The FDA product code for SUCTION REGULATOR 7700 SERIES is KDP.

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Related Devices (Code: KDP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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