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FDA 510(k)

COOK (R) VEIN GRAFT RING MARKERS

K-Number: K864101 · 1986-10-30

ApplicantCook, Inc.
Decision Date1986-10-30
Product CodeKPK
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

COOK (R) VEIN GRAFT RING MARKERS is the device name listed in this FDA 510(k) record. The listed applicant is Cook, Inc.. It received FDA 510(k) clearance on 1986-10-30 under 510(k) number K864101. The device is classified under product code KPK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COOK (R) VEIN GRAFT RING MARKERS?

COOK (R) VEIN GRAFT RING MARKERS is a medical device that received FDA 510(k) clearance on 1986-10-30. The listed applicant is Cook, Inc.. The 510(k) number is K864101.

When did COOK (R) VEIN GRAFT RING MARKERS receive FDA 510(k) clearance?

COOK (R) VEIN GRAFT RING MARKERS received FDA 510(k) clearance on 1986-10-30, under 510(k) number K864101.

Who is the listed applicant for COOK (R) VEIN GRAFT RING MARKERS?

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 COOK (R) VEIN GRAFT RING MARKERS?

The FDA product code for COOK (R) VEIN GRAFT RING MARKERS is KPK.

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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: KPK)

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.

K971966CORONARY VEIN GRAFT TAG MARKERMed-Edge, Inc.K895369VOSS GRAFT MARKERVoss Medical ProductsK864919SCANLAN (TM) VEIN/GRAFT HOLDERScanlan Intl., Inc.K801637FLUORO-MARK RADIOPAQUE ANATOMICAL MKR.C.R. Bard, Inc.K770802MARKERS, STAINLESS STEELCardio-Surgical, 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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