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FDA 510(k)

KENDALL CURITY SUCTION CATHETERS

K-Number: K892441 · 1989-05-31

ApplicantThe Kendal Co.
Decision Date1989-05-31
Product CodeBSY
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

KENDALL CURITY SUCTION CATHETERS 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 1989-05-31 under 510(k) number K892441. The device is classified under product code BSY. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KENDALL CURITY SUCTION CATHETERS?

KENDALL CURITY SUCTION CATHETERS is a medical device that received FDA 510(k) clearance on 1989-05-31. The listed applicant is The Kendal Co.. The 510(k) number is K892441.

When did KENDALL CURITY SUCTION CATHETERS receive FDA 510(k) clearance?

KENDALL CURITY SUCTION CATHETERS received FDA 510(k) clearance on 1989-05-31, under 510(k) number K892441.

Who is the listed applicant for KENDALL CURITY SUCTION CATHETERS?

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 SUCTION CATHETERS?

The FDA product code for KENDALL CURITY SUCTION CATHETERS is BSY.

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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 SETK951488KENDALL CURITY CATHETER PLUG WITH PROTECTIVE CAPK942664KENDALL MODEL 6325 SCD SEQUEL COMPRESSION SYSTEM

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Related Devices (Code: BSY)

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.

K031997MALLINCKRODT DAR TY-CARE / TY-CARE EXEL CLOSED SUCTION SYSTEMMallinckrodt Dar S.R.L.K992902AMBU HAND POWER SUCTION PUMPAmbu, Inc.K982945DUAL PURPOSE CLOSED CATHETERSpirit Medical Systems, Inc.K981910SUCTION CATHETERNi-Med, Inc.K972258HI-CARE CLOSED SUCTION SYSTEMMallinckrodt MedicalK973199AMSINO SUCTION CATHETERAmsino Intl., 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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