LIQUID AMYLASE REAGENT SET
K-Number: K930475 · 1993-07-19
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Device Summary
Frequently Asked Questions
What is the LIQUID AMYLASE REAGENT SET?
LIQUID AMYLASE REAGENT SET is a medical device that received FDA 510(k) clearance on 1993-07-19. The listed applicant is Pointe Scientific, Inc.,. The 510(k) number is K930475.
When did LIQUID AMYLASE REAGENT SET receive FDA 510(k) clearance?
LIQUID AMYLASE REAGENT SET received FDA 510(k) clearance on 1993-07-19, under 510(k) number K930475.
Who is the listed applicant for LIQUID AMYLASE REAGENT SET?
The FDA 510(k) record lists Pointe Scientific, Inc., as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIQUID AMYLASE REAGENT SET?
The FDA product code for LIQUID AMYLASE REAGENT SET 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 Pointe Scientific, 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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