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FDA 510(k)

CUSTOM WOUND MANAGEMENT KITS AND TRAYS

K-Number: K901856 · 1990-08-01

Decision Date1990-08-01
Product CodeLRO
Advisory CommitteeSU
DecisionUnknown

Device Summary

CUSTOM WOUND MANAGEMENT KITS AND TRAYS is the device name listed in this FDA 510(k) record. The listed applicant is Medcare Custom Packaging, Inc.. It received FDA 510(k) clearance on 1990-08-01 under 510(k) number K901856. 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 CUSTOM WOUND MANAGEMENT KITS AND TRAYS?

CUSTOM WOUND MANAGEMENT KITS AND TRAYS is a medical device that received FDA 510(k) clearance on 1990-08-01. The listed applicant is Medcare Custom Packaging, Inc.. The 510(k) number is K901856.

When did CUSTOM WOUND MANAGEMENT KITS AND TRAYS receive FDA 510(k) clearance?

CUSTOM WOUND MANAGEMENT KITS AND TRAYS received FDA 510(k) clearance on 1990-08-01, under 510(k) number K901856.

Who is the listed applicant for CUSTOM WOUND MANAGEMENT KITS AND TRAYS?

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

What is the FDA product code for CUSTOM WOUND MANAGEMENT KITS AND TRAYS?

The FDA product code for CUSTOM WOUND MANAGEMENT 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 Medcare Custom Packaging, 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 11 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

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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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