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FDA 510(k)

CLEARIUM, MOUNTING MEDIUM

K-Number: K830659 · 1983-03-17

ApplicantSurgipath Medical Industries, Inc.
Decision Date1983-03-17
Product CodeKEP
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

CLEARIUM, MOUNTING MEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is Surgipath Medical Industries, Inc.. It received FDA 510(k) clearance on 1983-03-17 under 510(k) number K830659. 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 CLEARIUM, MOUNTING MEDIUM?

CLEARIUM, MOUNTING MEDIUM is a medical device that received FDA 510(k) clearance on 1983-03-17. The listed applicant is Surgipath Medical Industries, Inc.. The 510(k) number is K830659.

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

CLEARIUM, MOUNTING MEDIUM received FDA 510(k) clearance on 1983-03-17, under 510(k) number K830659.

Who is the listed applicant for CLEARIUM, MOUNTING MEDIUM?

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

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

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

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Other records listing Surgipath Medical Industries, Inc. 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.

K883217SCHIFF REAGENTK881921C-E BRUSHK881922CYTOJARS PREFILLED WITH CYTOLOGY PRESERVATIVEK881659TISSUE SECTION ADHESIVEK863549REUSABLE/DISPOSABLE AUTOPSY KNIFE SETK863616KNIFE MAKER

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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.

K810323ACRYTOL, MOUNTING MEDIUMSurgipathK800847ENTELLANMcb Manufacturing Chemists, Inc.

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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