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)

TEKNO-MEDICAL OBSTETRICAL FORCEPS

K-Number: K013747 · 2002-02-11

ApplicantTekno Medical Optik-Chirurgie GmbH & Co.
Decision Date2002-02-11
Product CodeHDA
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TEKNO-MEDICAL OBSTETRICAL FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Tekno Medical Optik-Chirurgie GmbH & Co.. It received FDA 510(k) clearance on 2002-02-11 under 510(k) number K013747. The device is classified under product code HDA. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEKNO-MEDICAL OBSTETRICAL FORCEPS?

TEKNO-MEDICAL OBSTETRICAL FORCEPS is a medical device that received FDA 510(k) clearance on 2002-02-11. The listed applicant is Tekno Medical Optik-Chirurgie GmbH & Co.. The 510(k) number is K013747.

When did TEKNO-MEDICAL OBSTETRICAL FORCEPS receive FDA 510(k) clearance?

TEKNO-MEDICAL OBSTETRICAL FORCEPS received FDA 510(k) clearance on 2002-02-11, under 510(k) number K013747.

Who is the listed applicant for TEKNO-MEDICAL OBSTETRICAL FORCEPS?

The FDA 510(k) record lists Tekno Medical Optik-Chirurgie GmbH & Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TEKNO-MEDICAL OBSTETRICAL FORCEPS?

The FDA product code for TEKNO-MEDICAL OBSTETRICAL FORCEPS is HDA.

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 Tekno Medical Optik-Chirurgie GmbH & Co. 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.

K003717INSTRUMENTS FOR LAPAROSCOPY 5 MM, 10 MM WITH COLOURED HANDLE, DETACHABLE ENDODCOPIC INSTRUMENTS 5 MM, 10MM (HANDLE, SHAF

Related Devices (Code: HDA)

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.

K100517INSTRUMED FORCEPS OBSTERICAL, MODEL# 46-5XXX, OB-XXXXInstrumed International, Inc.K092827DIMELA OBSTERICAL FORCEPS, MODEL 72.1 XX XXDimeda Instrumente GmbHK951529V. MUELLER OBSTETRICAL (OB) FORCEPSBaxter Healthcare CorpK914552CMI VACUUM PUMPColumbia Medical & Surgical, Inc.K905583ILC FORCEPS PADSInman Liebelt Corp.K903205AUTO SUTURE(R) ENDOSCOPIC CLAMPUnited States Surgical, A Division of Tyco Healthc

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.

↑