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FDA 510(k)

CHARLES ENDOCOAGULATOR ACCESSORY FOR ARC

K-Number: K780851 · 1978-06-30

ApplicantVarian Assoc., Inc.
Decision Date1978-06-30
Product CodeHOB
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CHARLES ENDOCOAGULATOR ACCESSORY FOR ARC 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 1978-06-30 under 510(k) number K780851. The device is classified under product code HOB. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHARLES ENDOCOAGULATOR ACCESSORY FOR ARC?

CHARLES ENDOCOAGULATOR ACCESSORY FOR ARC is a medical device that received FDA 510(k) clearance on 1978-06-30. The listed applicant is Varian Assoc., Inc.. The 510(k) number is K780851.

When did CHARLES ENDOCOAGULATOR ACCESSORY FOR ARC receive FDA 510(k) clearance?

CHARLES ENDOCOAGULATOR ACCESSORY FOR ARC received FDA 510(k) clearance on 1978-06-30, under 510(k) number K780851.

Who is the listed applicant for CHARLES ENDOCOAGULATOR ACCESSORY FOR ARC?

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 CHARLES ENDOCOAGULATOR ACCESSORY FOR ARC?

The FDA product code for CHARLES ENDOCOAGULATOR ACCESSORY FOR ARC is HOB.

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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: HOB)

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.

K840310CATEGORY 6 OPTHALMIC DEVICESImm Enterprises , Ltd.K840101EYE SURGERY INSTRUMENTTruline Instruments, 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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