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FDA 510(k)

UNDERPAD CODE NO. 8453

K-Number: K760277 · 1976-08-11

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1976-08-11
Product CodeEYQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

UNDERPAD CODE NO. 8453 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 1976-08-11 under 510(k) number K760277. The device is classified under product code EYQ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNDERPAD CODE NO. 8453?

UNDERPAD CODE NO. 8453 is a medical device that received FDA 510(k) clearance on 1976-08-11. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K760277.

When did UNDERPAD CODE NO. 8453 receive FDA 510(k) clearance?

UNDERPAD CODE NO. 8453 received FDA 510(k) clearance on 1976-08-11, under 510(k) number K760277.

Who is the listed applicant for UNDERPAD CODE NO. 8453?

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 UNDERPAD CODE NO. 8453?

The FDA product code for UNDERPAD CODE NO. 8453 is EYQ.

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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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