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FDA 510(k)

I.V. START KIT (AHC-50-54954

K-Number: K924192 · 1993-08-27

Decision Date1993-08-27
Product CodeKGX
Advisory CommitteeHO
DecisionUnknown

Device Summary

I.V. START KIT (AHC-50-54954 is the device name listed in this FDA 510(k) record. The listed applicant is American Healthcare Corp.. It received FDA 510(k) clearance on 1993-08-27 under 510(k) number K924192. The device is classified under product code KGX. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the I.V. START KIT (AHC-50-54954?

I.V. START KIT (AHC-50-54954 is a medical device that received FDA 510(k) clearance on 1993-08-27. The listed applicant is American Healthcare Corp.. The 510(k) number is K924192.

When did I.V. START KIT (AHC-50-54954 receive FDA 510(k) clearance?

I.V. START KIT (AHC-50-54954 received FDA 510(k) clearance on 1993-08-27, under 510(k) number K924192.

Who is the listed applicant for I.V. START KIT (AHC-50-54954?

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

What is the FDA product code for I.V. START KIT (AHC-50-54954?

The FDA product code for I.V. START KIT (AHC-50-54954 is KGX.

Related Clinical Trials

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.

Other records listing American Healthcare 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.

View all 14 devices →

Related Devices (Code: KGX)

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.

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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