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FDA 510(k)

GLYCO-PROBE GSP

K-Number: K873428 · 1988-04-05

ApplicantIsolab, Inc.
Decision Date1988-04-05
Product CodeLCP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

GLYCO-PROBE GSP is the device name listed in this FDA 510(k) record. The listed applicant is Isolab, Inc.. It received FDA 510(k) clearance on 1988-04-05 under 510(k) number K873428. The device is classified under product code LCP. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GLYCO-PROBE GSP?

GLYCO-PROBE GSP is a medical device that received FDA 510(k) clearance on 1988-04-05. The listed applicant is Isolab, Inc.. The 510(k) number is K873428.

When did GLYCO-PROBE GSP receive FDA 510(k) clearance?

GLYCO-PROBE GSP received FDA 510(k) clearance on 1988-04-05, under 510(k) number K873428.

Who is the listed applicant for GLYCO-PROBE GSP?

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

What is the FDA product code for GLYCO-PROBE GSP?

The FDA product code for GLYCO-PROBE GSP is LCP.

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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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