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FDA 510(k)

FLEXIBLE MYOCARDIAL BIOPSY FORCEPS

K-Number: K883723 · 1988-12-05

ApplicantCook, Inc.
Decision Date1988-12-05
Product CodeDWZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

FLEXIBLE MYOCARDIAL BIOPSY FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Cook, Inc.. It received FDA 510(k) clearance on 1988-12-05 under 510(k) number K883723. The device is classified under product code DWZ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLEXIBLE MYOCARDIAL BIOPSY FORCEPS?

FLEXIBLE MYOCARDIAL BIOPSY FORCEPS is a medical device that received FDA 510(k) clearance on 1988-12-05. The listed applicant is Cook, Inc.. The 510(k) number is K883723.

When did FLEXIBLE MYOCARDIAL BIOPSY FORCEPS receive FDA 510(k) clearance?

FLEXIBLE MYOCARDIAL BIOPSY FORCEPS received FDA 510(k) clearance on 1988-12-05, under 510(k) number K883723.

Who is the listed applicant for FLEXIBLE MYOCARDIAL BIOPSY FORCEPS?

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 FLEXIBLE MYOCARDIAL BIOPSY FORCEPS?

The FDA product code for FLEXIBLE MYOCARDIAL BIOPSY FORCEPS is DWZ.

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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: DWZ)

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.

K252722Biopsy ForcepsFehling Instruments GmbHK170726Biopsy ForcepsFehling Instruments GmbH & Co. KGK072051NOVATOME, MODEL: SU101-50Scholten Surgical Instruments, Inc.K010473SPARROWHAWK DISPOSABLEAtc Technologies, Inc.K000409MODIFICATION TO T-REX BIOPSY FORCEPSBoston Scientific CorpK991486ULTRA-CBXMedcanica, 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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