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FDA 510(k)

VISC X-VITREOUS ASPIRATING & CUT. INSTR

K-Number: K760684 · 1976-10-05

ApplicantVarian Assoc., Inc.
Decision Date1976-10-05
Product CodeHKP
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

VISC X-VITREOUS ASPIRATING & CUT. INSTR is the device name listed in this FDA 510(k) record. The listed applicant is Varian Assoc., Inc.. It received FDA 510(k) clearance on 1976-10-05 under 510(k) number K760684. The device is classified under product code HKP. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISC X-VITREOUS ASPIRATING & CUT. INSTR?

VISC X-VITREOUS ASPIRATING & CUT. INSTR is a medical device that received FDA 510(k) clearance on 1976-10-05. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K760684.

When did VISC X-VITREOUS ASPIRATING & CUT. INSTR receive FDA 510(k) clearance?

VISC X-VITREOUS ASPIRATING & CUT. INSTR received FDA 510(k) clearance on 1976-10-05, under 510(k) number K760684.

Who is the listed applicant for VISC X-VITREOUS ASPIRATING & CUT. INSTR?

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

What is the FDA product code for VISC X-VITREOUS ASPIRATING & CUT. INSTR?

The FDA product code for VISC X-VITREOUS ASPIRATING & CUT. INSTR is HKP.

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Other records listing Varian Assoc., 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.

K000922PROTON VISIONK992762BRACHYVISION 6.0K992751SOMAVISIONK992753CADPLAN PLUS: 3D TREATMENT PLANNING SYSTEMK990085MILLENNIUM MLC -120K980601VARISOURCE WRIGHT VAGINAL CUFF APPLICATOR FOR VARIAN VARISOURCE REMOTE HIGH DOSE RATE AFTERIOADER

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Related Devices (Code: HKP)

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.

K952558AARON VAC 2Aaron Medical IndustriesK950056THE GRIESHABER AXIAL CUTTERGrieshaber & Co.K950287UNIVIT PROBEMedical Instrument Development Laboratories, Inc.K896622VISITEC VITRECTOMY UNITVisitec Co.K890595MENTOR ANTERIOR SEGMENT VITRECTORMentor O & O, Inc.K832074CAVITRON/KELMAN PHACO-EMULSIFIER ASPIRACooperVision, 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.

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