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FDA 510(k)

CORDIS BIPAL 7 BIOPSY FORCEPS

K-Number: K920289 · 1992-03-30

ApplicantCordis Corp.
Decision Date1992-03-30
Product CodeDWZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CORDIS BIPAL 7 BIOPSY FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1992-03-30 under 510(k) number K920289. 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 CORDIS BIPAL 7 BIOPSY FORCEPS?

CORDIS BIPAL 7 BIOPSY FORCEPS is a medical device that received FDA 510(k) clearance on 1992-03-30. The listed applicant is Cordis Corp.. The 510(k) number is K920289.

When did CORDIS BIPAL 7 BIOPSY FORCEPS receive FDA 510(k) clearance?

CORDIS BIPAL 7 BIOPSY FORCEPS received FDA 510(k) clearance on 1992-03-30, under 510(k) number K920289.

Who is the listed applicant for CORDIS BIPAL 7 BIOPSY FORCEPS?

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

What is the FDA product code for CORDIS BIPAL 7 BIOPSY FORCEPS?

The FDA product code for CORDIS BIPAL 7 BIOPSY FORCEPS is DWZ.

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Other records listing Cordis Corp. as applicant

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K112797POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETERK101651ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE, ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIREK082143MICRO GUIDE CATHETER XPK062798SMART NITINOL SELF-EXPANDING STENT, MODEL C06120MB, C07120MB, C08120MB, C06150MB, C07150MB, C08150MBK060877PALMAZ BLUE .014 TRANSHEPATIC BILIARY STENT SYSTEM-MODEL PB1550,BAS,BAX,PB1560,BAS,BAX,PB1850,BAS,BAXPB1860BAS,BAXK050645CORDIS AMIIA .014 PTA BALLOON CATHETER

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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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