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FDA 510(k)

CURITY I.V. START KIT

K-Number: K842898 · 1984-08-17

ApplicantThe Kendal Co.
Decision Date1984-08-17
Product CodeLRS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CURITY I.V. START KIT 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 1984-08-17 under 510(k) number K842898. The device is classified under product code LRS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CURITY I.V. START KIT?

CURITY I.V. START KIT is a medical device that received FDA 510(k) clearance on 1984-08-17. The listed applicant is The Kendal Co.. The 510(k) number is K842898.

When did CURITY I.V. START KIT receive FDA 510(k) clearance?

CURITY I.V. START KIT received FDA 510(k) clearance on 1984-08-17, under 510(k) number K842898.

Who is the listed applicant for CURITY I.V. START KIT?

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 CURITY I.V. START KIT?

The FDA product code for CURITY I.V. START KIT is LRS.

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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: LRS)

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.

K050654AMSINO I.V. START KITAmsino International, Inc.K001879INFUSION IV SETNirvi Intl. USAK963722IV START KITGrand Medical ProductsK951167EMS I.V. START KITEmergency Medical Supply, Inc.K950184B. BRAUN IV START KITSB. Braun of America, Inc.K944041PERSONAL HEARING SYSTEMResound Corp.

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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