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FDA 510(k)

DISPOSABLE 22MM ADAPTOR

K-Number: K791539 · 1979-09-07

Decision Date1979-09-07
Product CodeBZA
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE 22MM ADAPTOR is the device name listed in this FDA 510(k) record. The listed applicant is Hospitak, Inc.. It received FDA 510(k) clearance on 1979-09-07 under 510(k) number K791539. The device is classified under product code BZA. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE 22MM ADAPTOR?

DISPOSABLE 22MM ADAPTOR is a medical device that received FDA 510(k) clearance on 1979-09-07. The listed applicant is Hospitak, Inc.. The 510(k) number is K791539.

When did DISPOSABLE 22MM ADAPTOR receive FDA 510(k) clearance?

DISPOSABLE 22MM ADAPTOR received FDA 510(k) clearance on 1979-09-07, under 510(k) number K791539.

Who is the listed applicant for DISPOSABLE 22MM ADAPTOR?

The FDA 510(k) record lists Hospitak, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPOSABLE 22MM ADAPTOR?

The FDA product code for DISPOSABLE 22MM ADAPTOR is BZA.

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 Hospitak, Inc. 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 27 devices →

Related Devices (Code: BZA)

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

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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