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)

LAPAROSCOPIC INSTRUMENTS

K-Number: K925114 · 1994-02-28

ApplicantEndo Technic Corp.
Decision Date1994-02-28
Product CodeHFI
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

LAPAROSCOPIC INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Endo Technic Corp.. It received FDA 510(k) clearance on 1994-02-28 under 510(k) number K925114. The device is classified under product code HFI. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAPAROSCOPIC INSTRUMENTS?

LAPAROSCOPIC INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1994-02-28. The listed applicant is Endo Technic Corp.. The 510(k) number is K925114.

When did LAPAROSCOPIC INSTRUMENTS receive FDA 510(k) clearance?

LAPAROSCOPIC INSTRUMENTS received FDA 510(k) clearance on 1994-02-28, under 510(k) number K925114.

Who is the listed applicant for LAPAROSCOPIC INSTRUMENTS?

The FDA 510(k) record lists Endo Technic Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LAPAROSCOPIC INSTRUMENTS?

The FDA product code for LAPAROSCOPIC INSTRUMENTS is HFI.

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 Endo Technic 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.

K990908MILLENNIUMK971459DERMALASEK925079LAPAROSCOPIC INST. (SCISSORS,FORCEPS,NEEDLEHOLDER)K930756LAPAROSCOPIC IRRIGATION/ASPIRATION HANDPIECEK924058TROCARK9148251-125 ENDOSEED

View all 10 devices →

Related Devices (Code: HFI)

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.

K925960FORCEPS FOR LAPAROSCOPIC SURGERY OB/GYN USEZinnanti Surgical Instruments, Inc.K925957SCISSORS FOR LAPAROSCOPIC SURGERY OB/GYN USEZinnanti Surgical Instruments, Inc.K936026COOK LAPAROSCOPIC MINI RETRACTOR SETCook Urological, Inc.K924148DIAMOND-SHARP(R) TROCARSSnowden-PencerK930571REUSABLE HANDLE FOR LAPAROSCOPIC INST. W/ROTATINGNumed Technologies, Inc.K844053CANON 60 DEGREE FUNDUS CAMERA CF-60SCanon USA, 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.

↑