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FDA 510(k)

MUCOUS SPECIMEN TRAP

K-Number: K913643 · 1991-10-10

Decision Date1991-10-10
Product CodeBYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MUCOUS SPECIMEN TRAP is the device name listed in this FDA 510(k) record. The listed applicant is Medical Device Inspection Co., Inc.. It received FDA 510(k) clearance on 1991-10-10 under 510(k) number K913643. The device is classified under product code BYZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MUCOUS SPECIMEN TRAP?

MUCOUS SPECIMEN TRAP is a medical device that received FDA 510(k) clearance on 1991-10-10. The listed applicant is Medical Device Inspection Co., Inc.. The 510(k) number is K913643.

When did MUCOUS SPECIMEN TRAP receive FDA 510(k) clearance?

MUCOUS SPECIMEN TRAP received FDA 510(k) clearance on 1991-10-10, under 510(k) number K913643.

Who is the listed applicant for MUCOUS SPECIMEN TRAP?

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

What is the FDA product code for MUCOUS SPECIMEN TRAP?

The FDA product code for MUCOUS SPECIMEN TRAP is BYZ.

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 Medical Device Inspection Co., 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: BYZ)

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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