FDA 510(k)

QUIK-TEMP

K-Number: K800666 · 1980-05-08

Decision Date1980-05-08

Product CodeKPP

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

QUIK-TEMP is the device name listed in this FDA 510(k) record. The listed applicant is Liquid Crystal Products, Inc.. It received FDA 510(k) clearance on 1980-05-08 under 510(k) number K800666. The device is classified under product code KPP. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUIK-TEMP?

QUIK-TEMP is a medical device that received FDA 510(k) clearance on 1980-05-08. The listed applicant is Liquid Crystal Products, Inc.. The 510(k) number is K800666.

When did QUIK-TEMP receive FDA 510(k) clearance?

QUIK-TEMP received FDA 510(k) clearance on 1980-05-08, under 510(k) number K800666.

Who is the listed applicant for QUIK-TEMP?

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

What is the FDA product code for QUIK-TEMP?

The FDA product code for QUIK-TEMP is KPP.

Other records listing Liquid Crystal Products, 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.

K821312TEMPTREND TEMPERATURE TREND INDICATOR K800667MONITEMP BLOOD PACK TEMP. MONITOR

Related Devices (Code: KPP)

K812615TM-CAPDTri-Med, Inc.K803275KPP PERITONEAL DIALYSATE FILTERMillipore Corp.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.