ABBOTT SPECTRUM AMYLASE REAGENT
K-Number: K891241 · 1989-08-15
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Device Summary
Frequently Asked Questions
What is the ABBOTT SPECTRUM AMYLASE REAGENT?
ABBOTT SPECTRUM AMYLASE REAGENT is a medical device that received FDA 510(k) clearance on 1989-08-15. The listed applicant is Abbott Laboratories. The 510(k) number is K891241.
When did ABBOTT SPECTRUM AMYLASE REAGENT receive FDA 510(k) clearance?
ABBOTT SPECTRUM AMYLASE REAGENT received FDA 510(k) clearance on 1989-08-15, under 510(k) number K891241.
Who is the listed applicant for ABBOTT SPECTRUM AMYLASE REAGENT?
The FDA 510(k) record lists Abbott Laboratories as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ABBOTT SPECTRUM AMYLASE REAGENT?
The FDA product code for ABBOTT SPECTRUM AMYLASE REAGENT 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 Abbott Laboratories 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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