INFUSION FLUID WARMER
K-Number: K883873 · 1989-02-28
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Device Summary
Frequently Asked Questions
What is the INFUSION FLUID WARMER?
INFUSION FLUID WARMER is a medical device that received FDA 510(k) clearance on 1989-02-28. The listed applicant is Pmt Corp.. The 510(k) number is K883873.
When did INFUSION FLUID WARMER receive FDA 510(k) clearance?
INFUSION FLUID WARMER received FDA 510(k) clearance on 1989-02-28, under 510(k) number K883873.
Who is the listed applicant for INFUSION FLUID WARMER?
The FDA 510(k) record lists Pmt Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INFUSION FLUID WARMER?
The FDA product code for INFUSION FLUID WARMER is LGZ.
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 Pmt 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.
Related Devices (Code: LGZ)
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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