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FDA 510(k)

VARIOUS KITS AND TRAYS

K-Number: K920292 · 1994-01-26

Decision Date1994-01-26
Product CodeLRO
Advisory CommitteeSU
DecisionUnknown

Device Summary

VARIOUS KITS AND TRAYS is the device name listed in this FDA 510(k) record. The listed applicant is Professional Medical Products, Inc.. It received FDA 510(k) clearance on 1994-01-26 under 510(k) number K920292. The device is classified under product code LRO. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the VARIOUS KITS AND TRAYS?

VARIOUS KITS AND TRAYS is a medical device that received FDA 510(k) clearance on 1994-01-26. The listed applicant is Professional Medical Products, Inc.. The 510(k) number is K920292.

When did VARIOUS KITS AND TRAYS receive FDA 510(k) clearance?

VARIOUS KITS AND TRAYS received FDA 510(k) clearance on 1994-01-26, under 510(k) number K920292.

Who is the listed applicant for VARIOUS KITS AND TRAYS?

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

What is the FDA product code for VARIOUS KITS AND TRAYS?

The FDA product code for VARIOUS KITS AND TRAYS is LRO.

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 Professional Medical Products, 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 9 devices →

Related Devices (Code: LRO)

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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