ALBUMIN TEST (ALB) ITEM #65650
K-Number: K884705 · 1989-01-11
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Device Summary
Frequently Asked Questions
What is the ALBUMIN TEST (ALB) ITEM #65650?
ALBUMIN TEST (ALB) ITEM #65650 is a medical device that received FDA 510(k) clearance on 1989-01-11. The listed applicant is Em Diagnostic Systems, Inc.. The 510(k) number is K884705.
When did ALBUMIN TEST (ALB) ITEM #65650 receive FDA 510(k) clearance?
ALBUMIN TEST (ALB) ITEM #65650 received FDA 510(k) clearance on 1989-01-11, under 510(k) number K884705.
Who is the listed applicant for ALBUMIN TEST (ALB) ITEM #65650?
The FDA 510(k) record lists Em Diagnostic Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ALBUMIN TEST (ALB) ITEM #65650?
The FDA product code for ALBUMIN TEST (ALB) ITEM #65650 is CIX.
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 Em Diagnostic Systems, 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: CIX)
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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