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FDA 510(k)

CHENOWETH-FRANK RADIOPATHOLOGICAL GRID

K-Number: K933754 · 1993-09-20

ApplicantCook, Inc.
Decision Date1993-09-20
Product CodeIZH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CHENOWETH-FRANK RADIOPATHOLOGICAL GRID is the device name listed in this FDA 510(k) record. The listed applicant is Cook, Inc.. It received FDA 510(k) clearance on 1993-09-20 under 510(k) number K933754. The device is classified under product code IZH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHENOWETH-FRANK RADIOPATHOLOGICAL GRID?

CHENOWETH-FRANK RADIOPATHOLOGICAL GRID is a medical device that received FDA 510(k) clearance on 1993-09-20. The listed applicant is Cook, Inc.. The 510(k) number is K933754.

When did CHENOWETH-FRANK RADIOPATHOLOGICAL GRID receive FDA 510(k) clearance?

CHENOWETH-FRANK RADIOPATHOLOGICAL GRID received FDA 510(k) clearance on 1993-09-20, under 510(k) number K933754.

Who is the listed applicant for CHENOWETH-FRANK RADIOPATHOLOGICAL GRID?

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

What is the FDA product code for CHENOWETH-FRANK RADIOPATHOLOGICAL GRID?

The FDA product code for CHENOWETH-FRANK RADIOPATHOLOGICAL GRID is IZH.

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Other records listing Cook, 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.

K133634SPECTRUM TURBO-JECT PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER SETK132020ADVANCE 34LP LOW PROFILE PTA BALLOON DILATATION CATHETERK131201ENTUIT SECURE GASTROINTESTIONAL SUTURE ANCHOR SET, ENTUIT SECURE ADJUSTABLE GASTROINTESTINAL SUTURE ANCHOR SETK131206COOK CERVICAL RIPENING BALLOONK132334TURBO-JECT PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER (PICC) SETK122091COOK TURBO-FLO HD ACUTE HEMODIALYSIS CATHETER SET/TRAY COOK SPECTRUM TURBO-FLO HD ACUTE HEMODIALYSIS CATHETER SET/TRAY

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Related Devices (Code: IZH)

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.

K203509SMART FINDERIms Giotto S.P.A.K202294Affirm Contrast BiopsyHologic, Inc.K191495Biopsy PositionerFujifilm CorporationK161575Affirm Lateral Arm Upright Biopsy AccessoryHologicK161920Comfort CoverPrecision Dynamics CorporationK153486Affirm Prone Biopsy SystemHologic, 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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