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FDA 510(k)

MURDOCH LAPAROSCOPE LENS CLEANER

K-Number: K941092 · 1994-04-11

ApplicantCook, Inc.
Decision Date1994-04-11
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MURDOCH LAPAROSCOPE LENS CLEANER is the device name listed in this FDA 510(k) record. The listed applicant is Cook, Inc.. It received FDA 510(k) clearance on 1994-04-11 under 510(k) number K941092. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MURDOCH LAPAROSCOPE LENS CLEANER?

MURDOCH LAPAROSCOPE LENS CLEANER is a medical device that received FDA 510(k) clearance on 1994-04-11. The listed applicant is Cook, Inc.. The 510(k) number is K941092.

When did MURDOCH LAPAROSCOPE LENS CLEANER receive FDA 510(k) clearance?

MURDOCH LAPAROSCOPE LENS CLEANER received FDA 510(k) clearance on 1994-04-11, under 510(k) number K941092.

Who is the listed applicant for MURDOCH LAPAROSCOPE LENS CLEANER?

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 MURDOCH LAPAROSCOPE LENS CLEANER?

The FDA product code for MURDOCH LAPAROSCOPE LENS CLEANER is GCJ.

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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: GCJ)

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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