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FDA 510(k)

MICRA MICROSURGICAL INSTRUMENTS

K-Number: K862971 · 1986-08-25

ApplicantCordis Corp.
Decision Date1986-08-25
Product CodeGZX
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MICRA MICROSURGICAL INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Cordis Corp.. It received FDA 510(k) clearance on 1986-08-25 under 510(k) number K862971. The device is classified under product code GZX. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRA MICROSURGICAL INSTRUMENTS?

MICRA MICROSURGICAL INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1986-08-25. The listed applicant is Cordis Corp.. The 510(k) number is K862971.

When did MICRA MICROSURGICAL INSTRUMENTS receive FDA 510(k) clearance?

MICRA MICROSURGICAL INSTRUMENTS received FDA 510(k) clearance on 1986-08-25, under 510(k) number K862971.

Who is the listed applicant for MICRA MICROSURGICAL INSTRUMENTS?

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 MICRA MICROSURGICAL INSTRUMENTS?

The FDA product code for MICRA MICROSURGICAL INSTRUMENTS is GZX.

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Other records listing Cordis 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.

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: GZX)

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.

K932169MICROSURGICAL INSTRUMENTSAmerican Russian Medical Services, Inc.K926048CLARUS ENDOSCOPIC BALL PROBEClarus Medical Systems, Inc.K911932J105 JAMES SURGICAL SYSTEM I/A PACKO.R. Specialties, Inc.K890216MICROSURGICAL KERATOMEKinetic Medical ProductsK873933RANGE OF NEUROSURGICAL INSTRUMENTS IN TITANIUMDowns Surgical , Ltd.K873934RANGE OF CROCODILE ACTION INSTRUMENTSDowns Surgical , Ltd.

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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