FDA 510(k)

SORVALL EMBEDDING MEDIUM

K-Number: K760602 · 1976-09-21

ApplicantE.I. Dupont DE Nemours & Co., Inc.

Decision Date1976-09-21

Product CodeKEO

Advisory CommitteePA

DecisionSubstantially Equivalent

Device Summary

SORVALL EMBEDDING MEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. It received FDA 510(k) clearance on 1976-09-21 under 510(k) number K760602. The device is classified under product code KEO. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SORVALL EMBEDDING MEDIUM?

SORVALL EMBEDDING MEDIUM is a medical device that received FDA 510(k) clearance on 1976-09-21. The listed applicant is E.I. Dupont DE Nemours & Co., Inc.. The 510(k) number is K760602.

When did SORVALL EMBEDDING MEDIUM receive FDA 510(k) clearance?

SORVALL EMBEDDING MEDIUM received FDA 510(k) clearance on 1976-09-21, under 510(k) number K760602.

Who is the listed applicant for SORVALL EMBEDDING MEDIUM?

The FDA 510(k) record lists E.I. Dupont DE Nemours & Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SORVALL EMBEDDING MEDIUM?

The FDA product code for SORVALL EMBEDDING MEDIUM is KEO.

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Related Devices (Code: KEO)

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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.