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FDA 510(k)

LANCER PARAPLAST HISTO PROCESS CASSETTE

K-Number: K760623 · 1976-09-27

ApplicantSherwood Medical Industries
Decision Date1976-09-27
Product CodeIDZ
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

LANCER PARAPLAST HISTO PROCESS CASSETTE is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Industries. It received FDA 510(k) clearance on 1976-09-27 under 510(k) number K760623. 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 LANCER PARAPLAST HISTO PROCESS CASSETTE?

LANCER PARAPLAST HISTO PROCESS CASSETTE is a medical device that received FDA 510(k) clearance on 1976-09-27. The listed applicant is Sherwood Medical Industries. The 510(k) number is K760623.

When did LANCER PARAPLAST HISTO PROCESS CASSETTE receive FDA 510(k) clearance?

LANCER PARAPLAST HISTO PROCESS CASSETTE received FDA 510(k) clearance on 1976-09-27, under 510(k) number K760623.

Who is the listed applicant for LANCER PARAPLAST HISTO PROCESS CASSETTE?

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

What is the FDA product code for LANCER PARAPLAST HISTO PROCESS CASSETTE?

The FDA product code for LANCER PARAPLAST HISTO PROCESS CASSETTE is IDZ.

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Other records listing Sherwood Medical Industries 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.

K801070SHERWOOD DISPOSABLE ENDOMETRIAL SAMPLESK801071LANCER GLUCOSE RATE REAGENT KITK792014LANCER L-INA BUFFER, POLYMER, WASH SOLUK792013LANCER L-INA HUMAN REFERENCE SERUMK782077LANCER ICE CUBEK790523ARGYLE ESOPHAGEAL STETHOSCOPE

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Related Devices (Code: IDZ)

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.

K863483CASSETTE EMBOSSEERSurgipath Medical Industries, Inc.K862457LYNX EL MICROSCOPY TISSUE PROCESSORAustralian Biomedical Corporation , Ltd.K833857MACLEAN-FOGG, TISSUE CASSETTESPolymer Technology Corp.K831334TISSUE CASSETTES FOR PROCESSING-EM BEDSurgipath Medical Industries, 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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