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FDA 510(k)

BANDAGE COMPRESS 2, 3, 4

K-Number: K770410 · 1977-06-09

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1977-06-09
Product CodeNAB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BANDAGE COMPRESS 2, 3, 4 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 1977-06-09 under 510(k) number K770410. The device is classified under product code NAB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BANDAGE COMPRESS 2, 3, 4?

BANDAGE COMPRESS 2, 3, 4 is a medical device that received FDA 510(k) clearance on 1977-06-09. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K770410.

When did BANDAGE COMPRESS 2, 3, 4 receive FDA 510(k) clearance?

BANDAGE COMPRESS 2, 3, 4 received FDA 510(k) clearance on 1977-06-09, under 510(k) number K770410.

Who is the listed applicant for BANDAGE COMPRESS 2, 3, 4?

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 COMPRESS 2, 3, 4?

The FDA product code for BANDAGE COMPRESS 2, 3, 4 is NAB.

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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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