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FDA 510(k)

BANDAGE, TRIANGULAR NO. 8068

K-Number: K760250 · 1976-07-26

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1976-07-26
Product CodeILI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BANDAGE, TRIANGULAR NO. 8068 is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Professionals, Inc.. It received FDA 510(k) clearance on 1976-07-26 under 510(k) number K760250. The device is classified under product code ILI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BANDAGE, TRIANGULAR NO. 8068?

BANDAGE, TRIANGULAR NO. 8068 is a medical device that received FDA 510(k) clearance on 1976-07-26. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K760250.

When did BANDAGE, TRIANGULAR NO. 8068 receive FDA 510(k) clearance?

BANDAGE, TRIANGULAR NO. 8068 received FDA 510(k) clearance on 1976-07-26, under 510(k) number K760250.

Who is the listed applicant for BANDAGE, TRIANGULAR NO. 8068?

The FDA 510(k) record lists Johnson & Johnson Professionals, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BANDAGE, TRIANGULAR NO. 8068?

The FDA product code for BANDAGE, TRIANGULAR NO. 8068 is ILI.

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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.

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