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FDA 510(k)

BOEHRINGER LABORATORIES SUCTION INTERMITTOR

K-Number: K853095 · 1985-08-23

Decision Date1985-08-23
Product CodeGCX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BOEHRINGER LABORATORIES SUCTION INTERMITTOR is the device name listed in this FDA 510(k) record. The listed applicant is Boehringer Laboratories. It received FDA 510(k) clearance on 1985-08-23 under 510(k) number K853095. 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 BOEHRINGER LABORATORIES SUCTION INTERMITTOR?

BOEHRINGER LABORATORIES SUCTION INTERMITTOR is a medical device that received FDA 510(k) clearance on 1985-08-23. The listed applicant is Boehringer Laboratories. The 510(k) number is K853095.

When did BOEHRINGER LABORATORIES SUCTION INTERMITTOR receive FDA 510(k) clearance?

BOEHRINGER LABORATORIES SUCTION INTERMITTOR received FDA 510(k) clearance on 1985-08-23, under 510(k) number K853095.

Who is the listed applicant for BOEHRINGER LABORATORIES SUCTION INTERMITTOR?

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 LABORATORIES SUCTION INTERMITTOR?

The FDA product code for BOEHRINGER LABORATORIES SUCTION INTERMITTOR is GCX.

Related Clinical Trials

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.

Other records listing Boehringer Laboratories as applicant

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.

View all 38 devices →

Related Devices (Code: GCX)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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