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FDA 510(k)

DIATEK MODEL 700 THERMOMETER

K-Number: K895703 · 1989-12-07

ApplicantDiatek, Inc.
Decision Date1989-12-07
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DIATEK MODEL 700 THERMOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Diatek, Inc.. It received FDA 510(k) clearance on 1989-12-07 under 510(k) number K895703. 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 MODEL 700 THERMOMETER?

DIATEK MODEL 700 THERMOMETER is a medical device that received FDA 510(k) clearance on 1989-12-07. The listed applicant is Diatek, Inc.. The 510(k) number is K895703.

When did DIATEK MODEL 700 THERMOMETER receive FDA 510(k) clearance?

DIATEK MODEL 700 THERMOMETER received FDA 510(k) clearance on 1989-12-07, under 510(k) number K895703.

Who is the listed applicant for DIATEK MODEL 700 THERMOMETER?

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 MODEL 700 THERMOMETER?

The FDA product code for DIATEK MODEL 700 THERMOMETER 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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