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)

GMD UNIVERSAL CIRCUMCISION CLAMP, MODEL 200

K-Number: K063429 · 2007-01-17

ApplicantGeneric Medical Device, Inc.
Decision Date2007-01-17
Product CodeHFX
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

GMD UNIVERSAL CIRCUMCISION CLAMP, MODEL 200 is the device name listed in this FDA 510(k) record. The listed applicant is Generic Medical Device, Inc.. It received FDA 510(k) clearance on 2007-01-17 under 510(k) number K063429. The device is classified under product code HFX. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GMD UNIVERSAL CIRCUMCISION CLAMP, MODEL 200?

GMD UNIVERSAL CIRCUMCISION CLAMP, MODEL 200 is a medical device that received FDA 510(k) clearance on 2007-01-17. The listed applicant is Generic Medical Device, Inc.. The 510(k) number is K063429.

When did GMD UNIVERSAL CIRCUMCISION CLAMP, MODEL 200 receive FDA 510(k) clearance?

GMD UNIVERSAL CIRCUMCISION CLAMP, MODEL 200 received FDA 510(k) clearance on 2007-01-17, under 510(k) number K063429.

Who is the listed applicant for GMD UNIVERSAL CIRCUMCISION CLAMP, MODEL 200?

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

What is the FDA product code for GMD UNIVERSAL CIRCUMCISION CLAMP, MODEL 200?

The FDA product code for GMD UNIVERSAL CIRCUMCISION CLAMP, MODEL 200 is HFX.

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 Generic Medical Device, 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.

K111219GMD UNIVERSAL URINARY INCONTINENCE SLINGK083471GMD UNIVERSAL SLING, MODEL PRODUCT CODE 1010 AND 1020K070018UNIVERSAL SURGICAL MESH, MODEL 100

Related Devices (Code: HFX)

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.

K251687Konig Bell Circumcision ClampMedline Industries, LPK221356Wee BellWee MedicalK212911Konig Mogen ClampMedline Industries, Inc.K131373SHANGRINGWuhu Snnda Medical Treatment Appliance TechnologyK121789SHANGRINGWuhu Snna Medical Treatment Appliance Technology CK103695PREPEX SYSTEMCirc Medtech

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.

↑