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FDA 510(k)

HOT SHOT FLUID WARMER IV FLUIDS

K-Number: K992258 · 2000-01-12

Decision Date2000-01-12
Product CodeLDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HOT SHOT FLUID WARMER IV FLUIDS is the device name listed in this FDA 510(k) record. The listed applicant is Infra-Med Technologies, Inc.. It received FDA 510(k) clearance on 2000-01-12 under 510(k) number K992258. The device is classified under product code LDQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOT SHOT FLUID WARMER IV FLUIDS?

HOT SHOT FLUID WARMER IV FLUIDS is a medical device that received FDA 510(k) clearance on 2000-01-12. The listed applicant is Infra-Med Technologies, Inc.. The 510(k) number is K992258.

When did HOT SHOT FLUID WARMER IV FLUIDS receive FDA 510(k) clearance?

HOT SHOT FLUID WARMER IV FLUIDS received FDA 510(k) clearance on 2000-01-12, under 510(k) number K992258.

Who is the listed applicant for HOT SHOT FLUID WARMER IV FLUIDS?

The FDA 510(k) record lists Infra-Med Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HOT SHOT FLUID WARMER IV FLUIDS?

The FDA product code for HOT SHOT FLUID WARMER IV FLUIDS is LDQ.

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.

Related Devices (Code: LDQ)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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