VENTED/NON-VENTED GEMINI ADMINISTRATION SET
K-Number: K944320 · 1995-02-14
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Device Summary
Frequently Asked Questions
What is the VENTED/NON-VENTED GEMINI ADMINISTRATION SET?
VENTED/NON-VENTED GEMINI ADMINISTRATION SET is a medical device that received FDA 510(k) clearance on 1995-02-14. The listed applicant is Imed Corp.. The 510(k) number is K944320.
When did VENTED/NON-VENTED GEMINI ADMINISTRATION SET receive FDA 510(k) clearance?
VENTED/NON-VENTED GEMINI ADMINISTRATION SET received FDA 510(k) clearance on 1995-02-14, under 510(k) number K944320.
Who is the listed applicant for VENTED/NON-VENTED GEMINI ADMINISTRATION SET?
The FDA 510(k) record lists Imed Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VENTED/NON-VENTED GEMINI ADMINISTRATION SET?
The FDA product code for VENTED/NON-VENTED GEMINI ADMINISTRATION SET 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 Imed 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: 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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