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FDA 510(k)

CLINITEX VIS-X ASPIRATING ACCESSORY

K-Number: K780852 · 1978-11-03

ApplicantVarian Assoc., Inc.
Decision Date1978-11-03
Product CodeHKP
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CLINITEX VIS-X ASPIRATING ACCESSORY 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 1978-11-03 under 510(k) number K780852. 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 CLINITEX VIS-X ASPIRATING ACCESSORY?

CLINITEX VIS-X ASPIRATING ACCESSORY is a medical device that received FDA 510(k) clearance on 1978-11-03. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K780852.

When did CLINITEX VIS-X ASPIRATING ACCESSORY receive FDA 510(k) clearance?

CLINITEX VIS-X ASPIRATING ACCESSORY received FDA 510(k) clearance on 1978-11-03, under 510(k) number K780852.

Who is the listed applicant for CLINITEX VIS-X ASPIRATING ACCESSORY?

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 CLINITEX VIS-X ASPIRATING ACCESSORY?

The FDA product code for CLINITEX VIS-X ASPIRATING ACCESSORY 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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