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FDA 510(k)

BIOPSY PUNCH

K-Number: K896303 · 1990-02-13

ApplicantPremier Medical
Decision Date1990-02-13
Product CodeLRY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BIOPSY PUNCH is the device name listed in this FDA 510(k) record. The listed applicant is Premier Medical. It received FDA 510(k) clearance on 1990-02-13 under 510(k) number K896303. The device is classified under product code LRY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOPSY PUNCH?

BIOPSY PUNCH is a medical device that received FDA 510(k) clearance on 1990-02-13. The listed applicant is Premier Medical. The 510(k) number is K896303.

When did BIOPSY PUNCH receive FDA 510(k) clearance?

BIOPSY PUNCH received FDA 510(k) clearance on 1990-02-13, under 510(k) number K896303.

Who is the listed applicant for BIOPSY PUNCH?

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

What is the FDA product code for BIOPSY PUNCH?

The FDA product code for BIOPSY PUNCH is LRY.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Premier Medical 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.

K894050MODIFIED DECANNULATION STOPPERK884418PREMIER DIE-TRAK ARTICULATOR

Related Devices (Code: LRY)

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.

K933516ACU-E PUNCHAcuderm, Inc.K904869ELLIPSE PUNCHKramer ConstK902636LIPOGEN RHEUMELISA DSDNA ASSAYLipogen, Inc.K874356PIN PUNCHMed-Tool, Inc.K874357TAPERED PUNCHMed-Tool, Inc.K872388NAIL SETMed-Tool, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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