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FDA 510(k)

ADHESION PROMOTOR

K-Number: K760419 · 1976-08-23

ApplicantLee Pharmaceuticals
Decision Date1976-08-23
Product CodeEBD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ADHESION PROMOTOR is the device name listed in this FDA 510(k) record. The listed applicant is Lee Pharmaceuticals. It received FDA 510(k) clearance on 1976-08-23 under 510(k) number K760419. The device is classified under product code EBD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADHESION PROMOTOR?

ADHESION PROMOTOR is a medical device that received FDA 510(k) clearance on 1976-08-23. The listed applicant is Lee Pharmaceuticals. The 510(k) number is K760419.

When did ADHESION PROMOTOR receive FDA 510(k) clearance?

ADHESION PROMOTOR received FDA 510(k) clearance on 1976-08-23, under 510(k) number K760419.

Who is the listed applicant for ADHESION PROMOTOR?

The FDA 510(k) record lists Lee Pharmaceuticals as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ADHESION PROMOTOR?

The FDA product code for ADHESION PROMOTOR is EBD.

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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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