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FDA 510(k)

DIATEK 600 THERMOMETER SYSTEM

K-Number: K833568 · 1984-01-10

ApplicantDiatek, Inc.
Decision Date1984-01-10
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DIATEK 600 THERMOMETER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Diatek, Inc.. It received FDA 510(k) clearance on 1984-01-10 under 510(k) number K833568. 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 DIATEK 600 THERMOMETER SYSTEM?

DIATEK 600 THERMOMETER SYSTEM is a medical device that received FDA 510(k) clearance on 1984-01-10. The listed applicant is Diatek, Inc.. The 510(k) number is K833568.

When did DIATEK 600 THERMOMETER SYSTEM receive FDA 510(k) clearance?

DIATEK 600 THERMOMETER SYSTEM received FDA 510(k) clearance on 1984-01-10, under 510(k) number K833568.

Who is the listed applicant for DIATEK 600 THERMOMETER SYSTEM?

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 DIATEK 600 THERMOMETER SYSTEM?

The FDA product code for DIATEK 600 THERMOMETER SYSTEM is FLL.

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Other records listing Diatek, Inc. as applicant

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Related Devices (Code: FLL)

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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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