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FDA 510(k)

CUTTER JEL-ALGINATE IMPRESSION MAT.

K-Number: K760753 · 1976-10-20

ApplicantCutter Laboratories, Inc.
Decision Date1976-10-20
Product CodeELW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CUTTER JEL-ALGINATE IMPRESSION MAT. is the device name listed in this FDA 510(k) record. The listed applicant is Cutter Laboratories, Inc.. It received FDA 510(k) clearance on 1976-10-20 under 510(k) number K760753. 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 CUTTER JEL-ALGINATE IMPRESSION MAT.?

CUTTER JEL-ALGINATE IMPRESSION MAT. is a medical device that received FDA 510(k) clearance on 1976-10-20. The listed applicant is Cutter Laboratories, Inc.. The 510(k) number is K760753.

When did CUTTER JEL-ALGINATE IMPRESSION MAT. receive FDA 510(k) clearance?

CUTTER JEL-ALGINATE IMPRESSION MAT. received FDA 510(k) clearance on 1976-10-20, under 510(k) number K760753.

Who is the listed applicant for CUTTER JEL-ALGINATE IMPRESSION MAT.?

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

What is the FDA product code for CUTTER JEL-ALGINATE IMPRESSION MAT.?

The FDA product code for CUTTER JEL-ALGINATE IMPRESSION MAT. is ELW.

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Other records listing Cutter 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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