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FDA 510(k)

PASTE, ACCOE IMPRESSION

K-Number: K760226 · 1976-07-21

ApplicantCoe Laboratories, Inc.
Decision Date1976-07-21
Product CodeELW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PASTE, ACCOE IMPRESSION is the device name listed in this FDA 510(k) record. The listed applicant is Coe Laboratories, Inc.. It received FDA 510(k) clearance on 1976-07-21 under 510(k) number K760226. The device is classified under product code ELW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PASTE, ACCOE IMPRESSION?

PASTE, ACCOE IMPRESSION is a medical device that received FDA 510(k) clearance on 1976-07-21. The listed applicant is Coe Laboratories, Inc.. The 510(k) number is K760226.

When did PASTE, ACCOE IMPRESSION receive FDA 510(k) clearance?

PASTE, ACCOE IMPRESSION received FDA 510(k) clearance on 1976-07-21, under 510(k) number K760226.

Who is the listed applicant for PASTE, ACCOE IMPRESSION?

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

What is the FDA product code for PASTE, ACCOE IMPRESSION?

The FDA product code for PASTE, ACCOE IMPRESSION is ELW.

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Other records listing Coe Laboratories, Inc. as applicant

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Related Devices (Code: ELW)

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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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