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FDA 510(k)

I.V. START KIT, STERILE, DISPOSABLE

K-Number: K923361 · 1993-06-28

ApplicantTrinity Laboratories, Inc.
Decision Date1993-06-28
Product CodeLRS
Advisory CommitteeHO
DecisionUnknown

Device Summary

I.V. START KIT, STERILE, DISPOSABLE is the device name listed in this FDA 510(k) record. The listed applicant is Trinity Laboratories, Inc.. It received FDA 510(k) clearance on 1993-06-28 under 510(k) number K923361. The device is classified under product code LRS. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the I.V. START KIT, STERILE, DISPOSABLE?

I.V. START KIT, STERILE, DISPOSABLE is a medical device that received FDA 510(k) clearance on 1993-06-28. The listed applicant is Trinity Laboratories, Inc.. The 510(k) number is K923361.

When did I.V. START KIT, STERILE, DISPOSABLE receive FDA 510(k) clearance?

I.V. START KIT, STERILE, DISPOSABLE received FDA 510(k) clearance on 1993-06-28, under 510(k) number K923361.

Who is the listed applicant for I.V. START KIT, STERILE, DISPOSABLE?

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

What is the FDA product code for I.V. START KIT, STERILE, DISPOSABLE?

The FDA product code for I.V. START KIT, STERILE, DISPOSABLE is LRS.

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Other records listing Trinity Laboratories, Inc. as applicant

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K981441HEART CATH TRAY, STERILE, DISPOSABLEK974238DENTAL TRAY, STERILE, DISPOSABLEK974286CIRCUMCISION TRAY, CAT. NO. 70340K972160CRP-LEX SYSTEM: C-REACTIVE PROTEIN ANTIGEN DETECTION IN SERUM: SLIDE AGGLUTNATION LATEX TESTK970722EYE TRAYK965201O.R. SCRUB PREP TRAY, STERILE, DISPOSABLE

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Related Devices (Code: LRS)

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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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