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FDA 510(k)

PHASIX-HIGH FREQUENCY GENERATOR

K-Number: K834306 · 1983-12-29

ApplicantCgr Medical Corp.
Decision Date1983-12-29
Product CodeITY
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PHASIX-HIGH FREQUENCY GENERATOR is the device name listed in this FDA 510(k) record. The listed applicant is Cgr Medical Corp.. It received FDA 510(k) clearance on 1983-12-29 under 510(k) number K834306. The device is classified under product code ITY. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHASIX-HIGH FREQUENCY GENERATOR?

PHASIX-HIGH FREQUENCY GENERATOR is a medical device that received FDA 510(k) clearance on 1983-12-29. The listed applicant is Cgr Medical Corp.. The 510(k) number is K834306.

When did PHASIX-HIGH FREQUENCY GENERATOR receive FDA 510(k) clearance?

PHASIX-HIGH FREQUENCY GENERATOR received FDA 510(k) clearance on 1983-12-29, under 510(k) number K834306.

Who is the listed applicant for PHASIX-HIGH FREQUENCY GENERATOR?

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

What is the FDA product code for PHASIX-HIGH FREQUENCY GENERATOR?

The FDA product code for PHASIX-HIGH FREQUENCY GENERATOR is ITY.

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Other records listing Cgr Medical 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.

K843926PRESTILIX 1690K843235STENOSCOPK843985SUSPENSION 7K841649MAXIMAX - 4K833223SONEL 3000AK833941ORION

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Related Devices (Code: ITY)

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.

K000052X-RAY MONOBLOCK, MONOBLOCK XRS-60-330Dynarad Corp.K933162MRX-750Mrx Corp.K923094MOLYBDENUMSoutheastern Medical Diagnostics, Inc.K923141PHILIPS PRE-FILTER OPTIONPhilips Medical Systems, Inc.K921129MRX-700Mrx-Ray Tube Corp.K921130MRX-865Mrx-Ray Tube Corp.

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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