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FDA 510(k)

KIT PAK URINARY CARE SUPPLIES

K-Number: K925281 · 1993-04-19

ApplicantKit Pak, Inc.
Decision Date1993-04-19
Product CodeKNY
Advisory CommitteeGU
DecisionUnknown

Device Summary

KIT PAK URINARY CARE SUPPLIES is the device name listed in this FDA 510(k) record. The listed applicant is Kit Pak, Inc.. It received FDA 510(k) clearance on 1993-04-19 under 510(k) number K925281. The device is classified under product code KNY. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the KIT PAK URINARY CARE SUPPLIES?

KIT PAK URINARY CARE SUPPLIES is a medical device that received FDA 510(k) clearance on 1993-04-19. The listed applicant is Kit Pak, Inc.. The 510(k) number is K925281.

When did KIT PAK URINARY CARE SUPPLIES receive FDA 510(k) clearance?

KIT PAK URINARY CARE SUPPLIES received FDA 510(k) clearance on 1993-04-19, under 510(k) number K925281.

Who is the listed applicant for KIT PAK URINARY CARE SUPPLIES?

The FDA 510(k) record lists Kit Pak, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KIT PAK URINARY CARE SUPPLIES?

The FDA product code for KIT PAK URINARY CARE SUPPLIES is KNY.

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Other records listing Kit Pak, 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.

K942959KIT PAK WET SALINE DRESSINGK941499KIT PAK DRESSING CHANGE TRAYK932310KIT PAK INCONTINENT SKIN CARE KITK934080URINARY DRAINAGE BAGK931013FOLEY CATHETER TRAYK923905WOUND DRESSING KIT

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Related Devices (Code: KNY)

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.

K260919Transurethral Catheter Safety Valve (TUCSV) (80050)Class Medical , Ltd.K182144Bi-Flex EvoPromepla SamK162356Vesair Cystoscopic SheathSolace TherapeuticsK131803GUARDIAN URETHRAL SHEATHSolace TherapeuticsK123170VARI-PASS VARIABLE LENGTH ACCESS SHEATHOlympus Surgical Technologies AmericaK120160ROCAMED ROCAUS PLATINUMPromepla Sam

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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