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FDA 510(k)

COR-TEMP-TEMP. MONITOR

K-Number: K840675 · 1984-04-17

ApplicantProduct Research Organizations,Inc.
Decision Date1984-04-17
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

COR-TEMP-TEMP. MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Product Research Organizations,Inc.. It received FDA 510(k) clearance on 1984-04-17 under 510(k) number K840675. 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 COR-TEMP-TEMP. MONITOR?

COR-TEMP-TEMP. MONITOR is a medical device that received FDA 510(k) clearance on 1984-04-17. The listed applicant is Product Research Organizations,Inc.. The 510(k) number is K840675.

When did COR-TEMP-TEMP. MONITOR receive FDA 510(k) clearance?

COR-TEMP-TEMP. MONITOR received FDA 510(k) clearance on 1984-04-17, under 510(k) number K840675.

Who is the listed applicant for COR-TEMP-TEMP. MONITOR?

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

What is the FDA product code for COR-TEMP-TEMP. MONITOR?

The FDA product code for COR-TEMP-TEMP. MONITOR is FLL.

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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.

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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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