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FDA 510(k)

BAND AID* ADHESIVE BANDAGES

K-Number: K782003 · 1979-01-17

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1979-01-17
Product CodeFPX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BAND AID* ADHESIVE BANDAGES 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 1979-01-17 under 510(k) number K782003. The device is classified under product code FPX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BAND AID* ADHESIVE BANDAGES?

BAND AID* ADHESIVE BANDAGES is a medical device that received FDA 510(k) clearance on 1979-01-17. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K782003.

When did BAND AID* ADHESIVE BANDAGES receive FDA 510(k) clearance?

BAND AID* ADHESIVE BANDAGES received FDA 510(k) clearance on 1979-01-17, under 510(k) number K782003.

Who is the listed applicant for BAND AID* ADHESIVE BANDAGES?

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 BAND AID* ADHESIVE BANDAGES?

The FDA product code for BAND AID* ADHESIVE BANDAGES is FPX.

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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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