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FDA 510(k)

HI-LO TEMP(R) MODEL 8700 PATIENT TEMP MONITOR

K-Number: K874568 · 1988-01-06

Decision Date1988-01-06
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HI-LO TEMP(R) MODEL 8700 PATIENT TEMP MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Mallinckrodt Critical Care. It received FDA 510(k) clearance on 1988-01-06 under 510(k) number K874568. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HI-LO TEMP(R) MODEL 8700 PATIENT TEMP MONITOR?

HI-LO TEMP(R) MODEL 8700 PATIENT TEMP MONITOR is a medical device that received FDA 510(k) clearance on 1988-01-06. The listed applicant is Mallinckrodt Critical Care. The 510(k) number is K874568.

When did HI-LO TEMP(R) MODEL 8700 PATIENT TEMP MONITOR receive FDA 510(k) clearance?

HI-LO TEMP(R) MODEL 8700 PATIENT TEMP MONITOR received FDA 510(k) clearance on 1988-01-06, under 510(k) number K874568.

Who is the listed applicant for HI-LO TEMP(R) MODEL 8700 PATIENT TEMP MONITOR?

The FDA 510(k) record lists Mallinckrodt Critical Care as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HI-LO TEMP(R) MODEL 8700 PATIENT TEMP MONITOR?

The FDA product code for HI-LO TEMP(R) MODEL 8700 PATIENT TEMP MONITOR is FLL.

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 Mallinckrodt Critical Care 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.

View all 92 devices →

Related Devices (Code: FLL)

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

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

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