AMYLASE TEST
K-Number: K923677 · 1992-09-09
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Device Summary
Frequently Asked Questions
What is the AMYLASE TEST?
AMYLASE TEST is a medical device that received FDA 510(k) clearance on 1992-09-09. The listed applicant is Em Diagnostic Systems, Inc.. The 510(k) number is K923677.
When did AMYLASE TEST receive FDA 510(k) clearance?
AMYLASE TEST received FDA 510(k) clearance on 1992-09-09, under 510(k) number K923677.
Who is the listed applicant for AMYLASE TEST?
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 AMYLASE TEST?
The FDA product code for AMYLASE TEST is JFJ.
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: JFJ)
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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