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FDA 510(k)

I.V. START KIT

K-Number: K924811 · 1993-06-17

ApplicantTransidyne General Corp.
Decision Date1993-06-17
Product CodeLRS
Advisory CommitteeHO
DecisionUnknown

Device Summary

I.V. START KIT is the device name listed in this FDA 510(k) record. The listed applicant is Transidyne General Corp.. It received FDA 510(k) clearance on 1993-06-17 under 510(k) number K924811. 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?

I.V. START KIT is a medical device that received FDA 510(k) clearance on 1993-06-17. The listed applicant is Transidyne General Corp.. The 510(k) number is K924811.

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

I.V. START KIT received FDA 510(k) clearance on 1993-06-17, under 510(k) number K924811.

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

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

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

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

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Other records listing Transidyne General Corp. 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.

K961217BODILY FLUID DISPOSAL KITK955658LACERATION TRAYK950743ORAL PROCEDURE PACKK950773PROPHYLAXIS PACKK950449SURGICAL BURK950403SURGICAL SAW BLADES

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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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