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FDA 510(k)

ACC-U-THERM TEMPERATURE MONITOR

K-Number: K813468 · 1982-01-07

ApplicantDiatek, Inc.
Decision Date1982-01-07
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ACC-U-THERM TEMPERATURE MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Diatek, Inc.. It received FDA 510(k) clearance on 1982-01-07 under 510(k) number K813468. 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 ACC-U-THERM TEMPERATURE MONITOR?

ACC-U-THERM TEMPERATURE MONITOR is a medical device that received FDA 510(k) clearance on 1982-01-07. The listed applicant is Diatek, Inc.. The 510(k) number is K813468.

When did ACC-U-THERM TEMPERATURE MONITOR receive FDA 510(k) clearance?

ACC-U-THERM TEMPERATURE MONITOR received FDA 510(k) clearance on 1982-01-07, under 510(k) number K813468.

Who is the listed applicant for ACC-U-THERM TEMPERATURE MONITOR?

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

What is the FDA product code for ACC-U-THERM TEMPERATURE MONITOR?

The FDA product code for ACC-U-THERM TEMPERATURE 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 Diatek, 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.

View all 15 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

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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