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FDA 510(k)

STERILE MUCUS SPECIMEN TRAP, MODELS 406 & 407

K-Number: K875058 · 1988-02-12

Decision Date1988-02-12
Product CodeBSY
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

STERILE MUCUS SPECIMEN TRAP, MODELS 406 & 407 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 1988-02-12 under 510(k) number K875058. The device is classified under product code BSY. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILE MUCUS SPECIMEN TRAP, MODELS 406 & 407?

STERILE MUCUS SPECIMEN TRAP, MODELS 406 & 407 is a medical device that received FDA 510(k) clearance on 1988-02-12. The listed applicant is Busse Hospital Disposables, Inc.. The 510(k) number is K875058.

When did STERILE MUCUS SPECIMEN TRAP, MODELS 406 & 407 receive FDA 510(k) clearance?

STERILE MUCUS SPECIMEN TRAP, MODELS 406 & 407 received FDA 510(k) clearance on 1988-02-12, under 510(k) number K875058.

Who is the listed applicant for STERILE MUCUS SPECIMEN TRAP, MODELS 406 & 407?

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 STERILE MUCUS SPECIMEN TRAP, MODELS 406 & 407?

The FDA product code for STERILE MUCUS SPECIMEN TRAP, MODELS 406 & 407 is BSY.

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.

View all 31 devices →

Related Devices (Code: BSY)

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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