IVAC 52-99-0 UNVENTED & 52-99-1 VENTED VOL. INFUSI
K-Number: K844937 · 1985-01-25
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Device Summary
Frequently Asked Questions
What is the IVAC 52-99-0 UNVENTED & 52-99-1 VENTED VOL. INFUSI?
IVAC 52-99-0 UNVENTED & 52-99-1 VENTED VOL. INFUSI is a medical device that received FDA 510(k) clearance on 1985-01-25. The listed applicant is Y. The 510(k) number is K844937.
When did IVAC 52-99-0 UNVENTED & 52-99-1 VENTED VOL. INFUSI receive FDA 510(k) clearance?
IVAC 52-99-0 UNVENTED & 52-99-1 VENTED VOL. INFUSI received FDA 510(k) clearance on 1985-01-25, under 510(k) number K844937.
Who is the listed applicant for IVAC 52-99-0 UNVENTED & 52-99-1 VENTED VOL. INFUSI?
The FDA 510(k) record lists Y as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IVAC 52-99-0 UNVENTED & 52-99-1 VENTED VOL. INFUSI?
The FDA product code for IVAC 52-99-0 UNVENTED & 52-99-1 VENTED VOL. INFUSI is FPA.
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 Y 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: FPA)
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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