FDA 510(k)

TOURNIWRAP BANDAGE

K-Number: K760576 · 1976-10-05

Decision Date1976-10-05

Product CodeILG

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

TOURNIWRAP BANDAGE 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 K760576. The device is classified under product code ILG. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TOURNIWRAP BANDAGE?

TOURNIWRAP BANDAGE 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 K760576.

When did TOURNIWRAP BANDAGE receive FDA 510(k) clearance?

TOURNIWRAP BANDAGE received FDA 510(k) clearance on 1976-10-05, under 510(k) number K760576.

Who is the listed applicant for TOURNIWRAP BANDAGE?

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 TOURNIWRAP BANDAGE?

The FDA product code for TOURNIWRAP BANDAGE is ILG.

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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.