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FDA 510(k)

KENDALL CURITY CATHETER PLUG WITH PROTECTIVE CAP

K-Number: K951488 · 1995-04-25

ApplicantThe Kendal Co.
Decision Date1995-04-25
Product CodeKNY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

KENDALL CURITY CATHETER PLUG WITH PROTECTIVE CAP is the device name listed in this FDA 510(k) record. The listed applicant is The Kendal Co.. It received FDA 510(k) clearance on 1995-04-25 under 510(k) number K951488. The device is classified under product code KNY. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KENDALL CURITY CATHETER PLUG WITH PROTECTIVE CAP?

KENDALL CURITY CATHETER PLUG WITH PROTECTIVE CAP is a medical device that received FDA 510(k) clearance on 1995-04-25. The listed applicant is The Kendal Co.. The 510(k) number is K951488.

When did KENDALL CURITY CATHETER PLUG WITH PROTECTIVE CAP receive FDA 510(k) clearance?

KENDALL CURITY CATHETER PLUG WITH PROTECTIVE CAP received FDA 510(k) clearance on 1995-04-25, under 510(k) number K951488.

Who is the listed applicant for KENDALL CURITY CATHETER PLUG WITH PROTECTIVE CAP?

The FDA 510(k) record lists The Kendal Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KENDALL CURITY CATHETER PLUG WITH PROTECTIVE CAP?

The FDA product code for KENDALL CURITY CATHETER PLUG WITH PROTECTIVE CAP is KNY.

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Other records listing The Kendal Co. 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.

K000087MARHUKAR TRIPLE LUMEN CATHETER, MODEL 12 FRK990500KENDALL ULTRAMER COUDE FOLEY CATHETER, MODEL 1416C, KENDALL CURITY COUDE FOLEY CATHETER TRAY, MODEL 6946CK991758MONOJECT INSULIN SYRINGEK970969KENDALL CURITY SUPRAPUBIC CATHETER TRAY, KIT, & REPLACEMENT SETK942664KENDALL MODEL 6325 SCD SEQUEL COMPRESSION SYSTEMK942774POLYSKIN(R) M.R. MOIST RESPONSIVE TRANSPARENT DRESSING

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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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