MEDIQUIP I.A. FIELD CONV KIT/AMSCO 2080 SER TABLE
K-Number: K914417 · 1992-02-27
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Device Summary
Frequently Asked Questions
What is the MEDIQUIP I.A. FIELD CONV KIT/AMSCO 2080 SER TABLE?
MEDIQUIP I.A. FIELD CONV KIT/AMSCO 2080 SER TABLE is a medical device that received FDA 510(k) clearance on 1992-02-27. The listed applicant is Med-Vac, Inc.. The 510(k) number is K914417.
When did MEDIQUIP I.A. FIELD CONV KIT/AMSCO 2080 SER TABLE receive FDA 510(k) clearance?
MEDIQUIP I.A. FIELD CONV KIT/AMSCO 2080 SER TABLE received FDA 510(k) clearance on 1992-02-27, under 510(k) number K914417.
Who is the listed applicant for MEDIQUIP I.A. FIELD CONV KIT/AMSCO 2080 SER TABLE?
The FDA 510(k) record lists Med-Vac, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MEDIQUIP I.A. FIELD CONV KIT/AMSCO 2080 SER TABLE?
The FDA product code for MEDIQUIP I.A. FIELD CONV KIT/AMSCO 2080 SER TABLE is IXR.
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: IXR)
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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