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)

FORCEP, DISP., A CLAMP

K-Number: K771097 · 1977-07-14

ApplicantDravon Medical, Inc.
Decision Date1977-07-14
Product CodeHTD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FORCEP, DISP., A CLAMP is the device name listed in this FDA 510(k) record. The listed applicant is Dravon Medical, Inc.. It received FDA 510(k) clearance on 1977-07-14 under 510(k) number K771097. The device is classified under product code HTD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FORCEP, DISP., A CLAMP?

FORCEP, DISP., A CLAMP is a medical device that received FDA 510(k) clearance on 1977-07-14. The listed applicant is Dravon Medical, Inc.. The 510(k) number is K771097.

When did FORCEP, DISP., A CLAMP receive FDA 510(k) clearance?

FORCEP, DISP., A CLAMP received FDA 510(k) clearance on 1977-07-14, under 510(k) number K771097.

Who is the listed applicant for FORCEP, DISP., A CLAMP?

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

What is the FDA product code for FORCEP, DISP., A CLAMP?

The FDA product code for FORCEP, DISP., A CLAMP is HTD.

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 Dravon Medical, 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.

K873455S3086 ARTERIAL, S3087 VENOUS NEONATAL HEMODIALYSISK860770AM-100 I/A AMPACK832739STEDIFLO INFUSION SETK831842DRAVON T CLAMPK812771PERITONEAL DIALYSIS DRAINAGEK812772PERITONEAL DIALYSIS CYCLER SET (8UNIT)

View all 16 devices →

Related Devices (Code: HTD)

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.

K051281THE NEEDLE CATCHERE.D.Medical , Ltd.K974595CUSHING BAYONET, INSULATED BIPOLAR FORCEPTitan Mfg., Inc.K974594SEMKIN BIPOLAR FORCEPTitan Mfg., Inc.K974593SEMKIN INSULATED BIPOLAR FORCEPTitan Mfg., Inc.K913964MARLOW/REDDICK LAPAROSCOPIC GRASPING FORCEPSMarlo Surgical TechnologyK911180CLAW (5MM/10MM) ATRAUMATIC GRASP/MICRO FORCEPSNorthgate Technologies, 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.

↑