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FDA 510(k)

IMPROVED KNEE DRESSING

K-Number: K760573 · 1976-10-05

Decision Date1976-10-05
Product CodeITM
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

IMPROVED KNEE DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Richard'S Medical Equip., Inc.. It received FDA 510(k) clearance on 1976-10-05 under 510(k) number K760573. The device is classified under product code ITM. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMPROVED KNEE DRESSING?

IMPROVED KNEE DRESSING is a medical device that received FDA 510(k) clearance on 1976-10-05. The listed applicant is Richard'S Medical Equip., Inc.. The 510(k) number is K760573.

When did IMPROVED KNEE DRESSING receive FDA 510(k) clearance?

IMPROVED KNEE DRESSING received FDA 510(k) clearance on 1976-10-05, under 510(k) number K760573.

Who is the listed applicant for IMPROVED KNEE DRESSING?

The FDA 510(k) record lists Richard'S Medical Equip., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IMPROVED KNEE DRESSING?

The FDA product code for IMPROVED KNEE DRESSING is ITM.

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 Richard'S Medical Equip., 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 48 devices →

Related Devices (Code: ITM)

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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