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FDA 510(k)

LANCER BIOPSY HOLDER

K-Number: K772149 · 1977-11-22

ApplicantSherwood Medical Industries
Decision Date1977-11-22
Product CodeKER
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

LANCER BIOPSY HOLDER 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 1977-11-22 under 510(k) number K772149. The device is classified under product code KER. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LANCER BIOPSY HOLDER?

LANCER BIOPSY HOLDER is a medical device that received FDA 510(k) clearance on 1977-11-22. The listed applicant is Sherwood Medical Industries. The 510(k) number is K772149.

When did LANCER BIOPSY HOLDER receive FDA 510(k) clearance?

LANCER BIOPSY HOLDER received FDA 510(k) clearance on 1977-11-22, under 510(k) number K772149.

Who is the listed applicant for LANCER BIOPSY HOLDER?

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 BIOPSY HOLDER?

The FDA product code for LANCER BIOPSY HOLDER is KER.

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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: KER)

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.

K831922EMBEDDING RINGPolymer Technology Corp.K831900MACLEAN-FOGG, DISP. BASE MOLDPolymer Technology Corp.K831333EMBEDDING RINGSSurgipath Medical Industries, Inc.K831335DISPOSABLE BASE MOLDSurgipath 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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