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FDA 510(k)

INFECTIOUS DISEASE PROTECTION KIT, DISPOSABLE

K-Number: K874306 · 1988-03-22

Decision Date1988-03-22
Product CodeLGM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INFECTIOUS DISEASE PROTECTION KIT, DISPOSABLE is the device name listed in this FDA 510(k) record. The listed applicant is Busse Hospital Disposables, Inc.. It received FDA 510(k) clearance on 1988-03-22 under 510(k) number K874306. The device is classified under product code LGM. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INFECTIOUS DISEASE PROTECTION KIT, DISPOSABLE?

INFECTIOUS DISEASE PROTECTION KIT, DISPOSABLE is a medical device that received FDA 510(k) clearance on 1988-03-22. The listed applicant is Busse Hospital Disposables, Inc.. The 510(k) number is K874306.

When did INFECTIOUS DISEASE PROTECTION KIT, DISPOSABLE receive FDA 510(k) clearance?

INFECTIOUS DISEASE PROTECTION KIT, DISPOSABLE received FDA 510(k) clearance on 1988-03-22, under 510(k) number K874306.

Who is the listed applicant for INFECTIOUS DISEASE PROTECTION KIT, DISPOSABLE?

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

What is the FDA product code for INFECTIOUS DISEASE PROTECTION KIT, DISPOSABLE?

The FDA product code for INFECTIOUS DISEASE PROTECTION KIT, DISPOSABLE is LGM.

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 Busse Hospital Disposables, 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.

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Related Devices (Code: LGM)

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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