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FDA 510(k)

EVER-SHARP BIOPSY FORCEPS

K-Number: K895303 · 1990-01-16

ApplicantSouthwest Medical Mfg., Inc.
Decision Date1990-01-16
Product CodeHFB
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

EVER-SHARP BIOPSY FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Southwest Medical Mfg., Inc.. It received FDA 510(k) clearance on 1990-01-16 under 510(k) number K895303. The device is classified under product code HFB. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EVER-SHARP BIOPSY FORCEPS?

EVER-SHARP BIOPSY FORCEPS is a medical device that received FDA 510(k) clearance on 1990-01-16. The listed applicant is Southwest Medical Mfg., Inc.. The 510(k) number is K895303.

When did EVER-SHARP BIOPSY FORCEPS receive FDA 510(k) clearance?

EVER-SHARP BIOPSY FORCEPS received FDA 510(k) clearance on 1990-01-16, under 510(k) number K895303.

Who is the listed applicant for EVER-SHARP BIOPSY FORCEPS?

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

What is the FDA product code for EVER-SHARP BIOPSY FORCEPS?

The FDA product code for EVER-SHARP BIOPSY FORCEPS is HFB.

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 Southwest Medical Mfg., 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.

K922243E-Z CLAMP#1 AND#2

Related Devices (Code: HFB)

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.

K011488SPIRABRUSH CX BIOPSY INSTRUMENTTrylon Corp.K944444CIT BIOPSY PUNCHESChirurgische InstrumenteK930773SYMBIOSIS GYNECOLOGICAL BIOPSY FORCEPSSymbiosis Corp.K933767FORCEPS, BIOPSY GYNECOLOGICAL INSTRU/BIOPSYMahe-MedizintechnikK926595OWENS BIOPSY FORCEPSOwens Industries, Inc.K926527ROTO FIT BIOPSY FORCEPSThomasville Medical Assoc.

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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