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FDA 510(k)

BOEHRINGER LABS AMBULATORY PEEP VALVE

K-Number: K800755 · 1980-05-08

ApplicantBoehringer Laboratories
Decision Date1980-05-08
Product CodeBYE
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BOEHRINGER LABS AMBULATORY PEEP VALVE is the device name listed in this FDA 510(k) record. The listed applicant is Boehringer Laboratories. It received FDA 510(k) clearance on 1980-05-08 under 510(k) number K800755. The device is classified under product code BYE. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BOEHRINGER LABS AMBULATORY PEEP VALVE?

BOEHRINGER LABS AMBULATORY PEEP VALVE is a medical device that received FDA 510(k) clearance on 1980-05-08. The listed applicant is Boehringer Laboratories. The 510(k) number is K800755.

When did BOEHRINGER LABS AMBULATORY PEEP VALVE receive FDA 510(k) clearance?

BOEHRINGER LABS AMBULATORY PEEP VALVE received FDA 510(k) clearance on 1980-05-08, under 510(k) number K800755.

Who is the listed applicant for BOEHRINGER LABS AMBULATORY PEEP VALVE?

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 BOEHRINGER LABS AMBULATORY PEEP VALVE?

The FDA product code for BOEHRINGER LABS AMBULATORY PEEP VALVE is BYE.

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Related Devices (Code: BYE)

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.

K160112Besmed PEEP ValveBesmed Health Business CorpK122610PLAXTRON CPAP SYSTEM, MODEL CH-FFM-87XX/CH-FFM-88XX SERIESSen MU Technology Co., Ltd.K112546O_TWO CPAP SYSTEMO-Two Medical Technologies, Inc.K110713WATERPAP VALVEAirways Development, LLCK103833NEOPIP PATIENT CIRCUIT WITH PEEPNeoforce Group, Inc.K092029VENTSTAR RESUSCITAIRE, MODEL MP00311, VENTSTAR RESUSCITAIRE CEU, MODEL MP00310Draeger Medical AG & Co. KG

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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