FDA 510(k)

CASSETTE EMBOSSEER

K-Number: K863483 · 1986-09-16

ApplicantSurgipath Medical Industries, Inc.

Decision Date1986-09-16

Product CodeIDZ

Advisory CommitteePA

DecisionSubstantially Equivalent

Device Summary

CASSETTE EMBOSSEER 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 1986-09-16 under 510(k) number K863483. The device is classified under product code IDZ. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CASSETTE EMBOSSEER?

CASSETTE EMBOSSEER is a medical device that received FDA 510(k) clearance on 1986-09-16. The listed applicant is Surgipath Medical Industries, Inc.. The 510(k) number is K863483.

When did CASSETTE EMBOSSEER receive FDA 510(k) clearance?

CASSETTE EMBOSSEER received FDA 510(k) clearance on 1986-09-16, under 510(k) number K863483.

Who is the listed applicant for CASSETTE EMBOSSEER?

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 CASSETTE EMBOSSEER?

The FDA product code for CASSETTE EMBOSSEER is IDZ.

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Other records listing Surgipath Medical Industries, Inc. as applicant

K883217SCHIFF REAGENT K881921C-E BRUSH K881922CYTOJARS PREFILLED WITH CYTOLOGY PRESERVATIVE K881659TISSUE SECTION ADHESIVE K863549REUSABLE/DISPOSABLE AUTOPSY KNIFE SET K863616KNIFE MAKER

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Related Devices (Code: IDZ)

K862457LYNX EL MICROSCOPY TISSUE PROCESSORAustralian Biomedical Corporation , Ltd.K833857MACLEAN-FOGG, TISSUE CASSETTESPolymer Technology Corp.K831334TISSUE CASSETTES FOR PROCESSING-EM BEDSurgipath Medical Industries, Inc.K760623LANCER PARAPLAST HISTO PROCESS CASSETTESherwood Medical Industries

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.