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FDA 510(k)

MAGNET RETRIEVAL CATHETER

K-Number: K900852 · 1990-05-02

ApplicantCook, Inc.
Decision Date1990-05-02
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MAGNET RETRIEVAL CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Cook, Inc.. It received FDA 510(k) clearance on 1990-05-02 under 510(k) number K900852. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAGNET RETRIEVAL CATHETER?

MAGNET RETRIEVAL CATHETER is a medical device that received FDA 510(k) clearance on 1990-05-02. The listed applicant is Cook, Inc.. The 510(k) number is K900852.

When did MAGNET RETRIEVAL CATHETER receive FDA 510(k) clearance?

MAGNET RETRIEVAL CATHETER received FDA 510(k) clearance on 1990-05-02, under 510(k) number K900852.

Who is the listed applicant for MAGNET RETRIEVAL CATHETER?

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 MAGNET RETRIEVAL CATHETER?

The FDA product code for MAGNET RETRIEVAL CATHETER is KNT.

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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: KNT)

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.

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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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