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)

PFISTER-SCHWARTZ STONE RETRIEVER

K-Number: K771302 · 1977-08-02

ApplicantV. Mueller O.V. Baxter Healthcare Corp.
Decision Date1977-08-02
Product CodeFGO
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PFISTER-SCHWARTZ STONE RETRIEVER 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 1977-08-02 under 510(k) number K771302. The device is classified under product code FGO. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PFISTER-SCHWARTZ STONE RETRIEVER?

PFISTER-SCHWARTZ STONE RETRIEVER is a medical device that received FDA 510(k) clearance on 1977-08-02. The listed applicant is V. Mueller O.V. Baxter Healthcare Corp.. The 510(k) number is K771302.

When did PFISTER-SCHWARTZ STONE RETRIEVER receive FDA 510(k) clearance?

PFISTER-SCHWARTZ STONE RETRIEVER received FDA 510(k) clearance on 1977-08-02, under 510(k) number K771302.

Who is the listed applicant for PFISTER-SCHWARTZ STONE RETRIEVER?

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 PFISTER-SCHWARTZ STONE RETRIEVER?

The FDA product code for PFISTER-SCHWARTZ STONE RETRIEVER is FGO.

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 ENDOTRACHEALK770959BOUGIE, FILIFORM, JACKSONK770280CORD, ELECTROSURGICAL-STERILE & DISPOS.K760851CONVERSE ALTAR RETRACTOR

View all 41 devices →

Related Devices (Code: FGO)

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.

K001563SCIPRO(TM) FLEXIBLE STONE DISLODGER AND RETRIEVAL SETScion Cardiovascular, Inc.K970121STONE DISLODGER, BASKETBoston Scientific CorpK963750RETRIEVAL SNAREBoston Scientific CorpK962676DISPOSABLE ENDOSCOPIC RETRIEVAL DEVICEUnited States Endoscopy Group, Inc.K951309STONE DISLODGER, BASKETBoston Scientific CorpK933261GRASPING FORCEPSSurgitek

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.

↑