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FDA 510(k)

CUSTOM PROCEDURE TRAYS

K-Number: K871616 · 1987-12-11

Decision Date1987-12-11
Product CodeFMF
Advisory CommitteeHO
DecisionUnknown

Device Summary

CUSTOM PROCEDURE TRAYS is the device name listed in this FDA 510(k) record. The listed applicant is Medical Custom Products, Inc.. It received FDA 510(k) clearance on 1987-12-11 under 510(k) number K871616. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the CUSTOM PROCEDURE TRAYS?

CUSTOM PROCEDURE TRAYS is a medical device that received FDA 510(k) clearance on 1987-12-11. The listed applicant is Medical Custom Products, Inc.. The 510(k) number is K871616.

When did CUSTOM PROCEDURE TRAYS receive FDA 510(k) clearance?

CUSTOM PROCEDURE TRAYS received FDA 510(k) clearance on 1987-12-11, under 510(k) number K871616.

Who is the listed applicant for CUSTOM PROCEDURE TRAYS?

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

What is the FDA product code for CUSTOM PROCEDURE TRAYS?

The FDA product code for CUSTOM PROCEDURE TRAYS is FMF.

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.

Related Devices (Code: FMF)

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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