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FDA 510(k)

ASO SURE PLUS

K-Number: K820786 · 1982-04-08

ApplicantAnalytical Products, Inc.
Decision Date1982-04-08
Product CodeGTQ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ASO SURE PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Analytical Products, Inc.. It received FDA 510(k) clearance on 1982-04-08 under 510(k) number K820786. The device is classified under product code GTQ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASO SURE PLUS?

ASO SURE PLUS is a medical device that received FDA 510(k) clearance on 1982-04-08. The listed applicant is Analytical Products, Inc.. The 510(k) number is K820786.

When did ASO SURE PLUS receive FDA 510(k) clearance?

ASO SURE PLUS received FDA 510(k) clearance on 1982-04-08, under 510(k) number K820786.

Who is the listed applicant for ASO SURE PLUS?

The FDA 510(k) record lists Analytical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ASO SURE PLUS?

The FDA product code for ASO SURE PLUS is GTQ.

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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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