SEAC MOBILE UNIT BY ASI MEDICAL
K-Number: K932873 · 1994-03-07
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Device Summary
Frequently Asked Questions
What is the SEAC MOBILE UNIT BY ASI MEDICAL?
SEAC MOBILE UNIT BY ASI MEDICAL is a medical device that received FDA 510(k) clearance on 1994-03-07. The listed applicant is Asi Medical, Inc.. The 510(k) number is K932873.
When did SEAC MOBILE UNIT BY ASI MEDICAL receive FDA 510(k) clearance?
SEAC MOBILE UNIT BY ASI MEDICAL received FDA 510(k) clearance on 1994-03-07, under 510(k) number K932873.
Who is the listed applicant for SEAC MOBILE UNIT BY ASI MEDICAL?
The FDA 510(k) record lists Asi Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SEAC MOBILE UNIT BY ASI MEDICAL?
The FDA product code for SEAC MOBILE UNIT BY ASI MEDICAL is EIA.
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 Asi Medical, Inc. 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: EIA)
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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