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FDA 510(k)

MONITEMP BLOOD PACK TEMP. MONITOR

K-Number: K800667 · 1980-04-16

ApplicantLiquid Crystal Products, Inc.
Decision Date1980-04-16
Product CodeKSE
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

MONITEMP BLOOD PACK TEMP. MONITOR 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 1980-04-16 under 510(k) number K800667. The device is classified under product code KSE. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MONITEMP BLOOD PACK TEMP. MONITOR?

MONITEMP BLOOD PACK TEMP. MONITOR is a medical device that received FDA 510(k) clearance on 1980-04-16. The listed applicant is Liquid Crystal Products, Inc.. The 510(k) number is K800667.

When did MONITEMP BLOOD PACK TEMP. MONITOR receive FDA 510(k) clearance?

MONITEMP BLOOD PACK TEMP. MONITOR received FDA 510(k) clearance on 1980-04-16, under 510(k) number K800667.

Who is the listed applicant for MONITEMP BLOOD PACK TEMP. MONITOR?

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 MONITEMP BLOOD PACK TEMP. MONITOR?

The FDA product code for MONITEMP BLOOD PACK TEMP. MONITOR is KSE.

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.

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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 INDICATORK800666QUIK-TEMP

Related Devices (Code: KSE)

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.

K884436MODIFIED LOW-TEMP. FREEZER MODEL HLT-80LS-85Harris Mfg. Co.K813327SEPCOR TEMPERATURE MONITORSeparation Science Corp.K802319HEMOTEMP TMMarion Laboratories, Inc.

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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