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)

OPHTHALMIC SURGICAL PNEUMATIC SCISSORS DRIVER

K-Number: K932668 · 1994-02-23

ApplicantSynergetics, Inc.
Decision Date1994-02-23
Product CodeHQE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OPHTHALMIC SURGICAL PNEUMATIC SCISSORS DRIVER is the device name listed in this FDA 510(k) record. The listed applicant is Synergetics, Inc.. It received FDA 510(k) clearance on 1994-02-23 under 510(k) number K932668. The device is classified under product code HQE. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPHTHALMIC SURGICAL PNEUMATIC SCISSORS DRIVER?

OPHTHALMIC SURGICAL PNEUMATIC SCISSORS DRIVER is a medical device that received FDA 510(k) clearance on 1994-02-23. The listed applicant is Synergetics, Inc.. The 510(k) number is K932668.

When did OPHTHALMIC SURGICAL PNEUMATIC SCISSORS DRIVER receive FDA 510(k) clearance?

OPHTHALMIC SURGICAL PNEUMATIC SCISSORS DRIVER received FDA 510(k) clearance on 1994-02-23, under 510(k) number K932668.

Who is the listed applicant for OPHTHALMIC SURGICAL PNEUMATIC SCISSORS DRIVER?

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

What is the FDA product code for OPHTHALMIC SURGICAL PNEUMATIC SCISSORS DRIVER?

The FDA product code for OPHTHALMIC SURGICAL PNEUMATIC SCISSORS DRIVER is HQE.

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 Synergetics, 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.

K121426AYNERGETICS DISPOSABLE SPETZLER-MALIS STANDARD BIPOLAR FORCEPSK121675VERSAVITK113857SYNERGETICS DIRECTIONAL ENDOOCULAR LASER PROBEK110924DISPOSABLE SPETZLER-MALIS DUAL IRRIGATING BIPOLAR FORCEPSK091441SYNERGETICS ADJUSTABLE GAS PRESSURIZED INFUSION (AGPI) TUBE SETK071482STRYKER RF MULTI-LESION GENERATOR, MODEL 0406-900-000

View all 16 devices →

Related Devices (Code: HQE)

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.

K212763UniVit HE, UniVit UHSVisioncare Devices, LLCK170183Cetus system, Cetus probeA.R.C Laser GmbHK153168Bi-Blade Vitrectomy CutterMedical Instrument Development LaboratoriesK121675VERSAVITSynergetics, Inc.K120170PROCARE PLUS VITRECTOMY SYSTEMVisioncare Devices, Inc.K102222ULTIMATE VIT ENHAMCER (UVE)Medical Instrument Development Laboratories, 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.

↑