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FDA 510(k)

PRESTILIX 1690

K-Number: K843926 · 1984-12-17

ApplicantCgr Medical Corp.
Decision Date1984-12-17
Product CodeIXR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PRESTILIX 1690 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 1984-12-17 under 510(k) number K843926. The device is classified under product code IXR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRESTILIX 1690?

PRESTILIX 1690 is a medical device that received FDA 510(k) clearance on 1984-12-17. The listed applicant is Cgr Medical Corp.. The 510(k) number is K843926.

When did PRESTILIX 1690 receive FDA 510(k) clearance?

PRESTILIX 1690 received FDA 510(k) clearance on 1984-12-17, under 510(k) number K843926.

Who is the listed applicant for PRESTILIX 1690?

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 PRESTILIX 1690?

The FDA product code for PRESTILIX 1690 is IXR.

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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.

K843235STENOSCOPK843985SUSPENSION 7K841649MAXIMAX - 4K833223SONEL 3000AK833941ORIONK834306PHASIX-HIGH FREQUENCY GENERATOR

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Related Devices (Code: IXR)

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.

K000412VISION R/F TILTING TABLEVilla Sistemi Medicali S.P.A.K973039LEGACY/LEGACY-D TABLEGE Medical SystemsK971128CAP-35B III/CINE 275Jamieson Film Co.K970640PHILIPS EASY DIAGNOSTPhilips Medical Systems North America, Inc.K965105ELECTROPHYSIOLOGY TILT TABLE MODEL #9660U.S. Imaging Tables, Inc.K965096FLUOROVIEW SERIES FLUOROSCOPIC TABLESU.S. Imaging Tables, 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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