Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

FLEXIBLE BIOPSY FORCEPS

K-Number: K760717 · 1976-10-21

ApplicantV. Mueller O.V. Baxter Healthcare Corp.
Decision Date1976-10-21
Product CodeKOA
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FLEXIBLE BIOPSY FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is V. Mueller O.V. Baxter Healthcare Corp.. It received FDA 510(k) clearance on 1976-10-21 under 510(k) number K760717. The device is classified under product code KOA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLEXIBLE BIOPSY FORCEPS?

FLEXIBLE BIOPSY FORCEPS is a medical device that received FDA 510(k) clearance on 1976-10-21. The listed applicant is V. Mueller O.V. Baxter Healthcare Corp.. The 510(k) number is K760717.

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

FLEXIBLE BIOPSY FORCEPS received FDA 510(k) clearance on 1976-10-21, under 510(k) number K760717.

Who is the listed applicant for FLEXIBLE BIOPSY FORCEPS?

The FDA 510(k) record lists V. Mueller O.V. Baxter Healthcare Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLEXIBLE BIOPSY FORCEPS?

The FDA product code for FLEXIBLE BIOPSY FORCEPS is KOA.

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 V. Mueller O.V. Baxter Healthcare Corp. 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.

K803292FIELD SUCTION DISSECTORK792383KELMAN DIPSTICKK771197NORTON ENDOTRACHEALK771302PFISTER-SCHWARTZ STONE RETRIEVERK770959BOUGIE, FILIFORM, JACKSONK770280CORD, ELECTROSURGICAL-STERILE & DISPOS.

View all 41 devices →

Related Devices (Code: KOA)

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.

K182664FiXcisionAgency For Medical Innovations GmbHK950267URETHRAL SUTURE GUIDEApplied Medical ResourcesK932465LI VASECTOMYFemcare , Ltd.K921546VASOVASOSTOMY SETCook Urological, Inc.K931181VESITEC SUTURE PASSERVesitec Medical, Inc.K921304DDV LIGATORNorth American Medical, 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.

↑