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FDA 510(k)

ACRYTOL, MOUNTING MEDIUM

K-Number: K810323 · 1981-03-06

ApplicantSurgipath
Decision Date1981-03-06
Product CodeKEP
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

ACRYTOL, MOUNTING MEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is Surgipath. It received FDA 510(k) clearance on 1981-03-06 under 510(k) number K810323. The device is classified under product code KEP. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACRYTOL, MOUNTING MEDIUM?

ACRYTOL, MOUNTING MEDIUM is a medical device that received FDA 510(k) clearance on 1981-03-06. The listed applicant is Surgipath. The 510(k) number is K810323.

When did ACRYTOL, MOUNTING MEDIUM receive FDA 510(k) clearance?

ACRYTOL, MOUNTING MEDIUM received FDA 510(k) clearance on 1981-03-06, under 510(k) number K810323.

Who is the listed applicant for ACRYTOL, MOUNTING MEDIUM?

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

What is the FDA product code for ACRYTOL, MOUNTING MEDIUM?

The FDA product code for ACRYTOL, MOUNTING MEDIUM is KEP.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Surgipath as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 12 devices →

Related Devices (Code: KEP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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