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FDA 510(k)

VASCULAR BIOPSY FORCEPS

K-Number: K910840 · 1991-07-15

ApplicantVascular Products, Inc.
Decision Date1991-07-15
Product CodeDWZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VASCULAR BIOPSY FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Vascular Products, Inc.. It received FDA 510(k) clearance on 1991-07-15 under 510(k) number K910840. The device is classified under product code DWZ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VASCULAR BIOPSY FORCEPS?

VASCULAR BIOPSY FORCEPS is a medical device that received FDA 510(k) clearance on 1991-07-15. The listed applicant is Vascular Products, Inc.. The 510(k) number is K910840.

When did VASCULAR BIOPSY FORCEPS receive FDA 510(k) clearance?

VASCULAR BIOPSY FORCEPS received FDA 510(k) clearance on 1991-07-15, under 510(k) number K910840.

Who is the listed applicant for VASCULAR BIOPSY FORCEPS?

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

What is the FDA product code for VASCULAR BIOPSY FORCEPS?

The FDA product code for VASCULAR BIOPSY FORCEPS is DWZ.

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 Vascular Products, 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.

K913733STERILE CHEST TUBEK823447IMPLANTABLE PACING LEAD, TINED #3262 &

Related Devices (Code: DWZ)

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.

K252722Biopsy ForcepsFehling Instruments GmbHK170726Biopsy ForcepsFehling Instruments GmbH & Co. KGK072051NOVATOME, MODEL: SU101-50Scholten Surgical Instruments, Inc.K010473SPARROWHAWK DISPOSABLEAtc Technologies, Inc.K000409MODIFICATION TO T-REX BIOPSY FORCEPSBoston Scientific CorpK991486ULTRA-CBXMedcanica, 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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