FDA 510(k)

THERMOMETER, DIGITAL FEVER (MEDITEMP)

K-Number: K760118 · 1976-07-20

ApplicantJohnson & Johnson Professionals, Inc.

Decision Date1976-07-20

Product CodeFLL

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

THERMOMETER, DIGITAL FEVER (MEDITEMP) is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Professionals, Inc.. It received FDA 510(k) clearance on 1976-07-20 under 510(k) number K760118. 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 THERMOMETER, DIGITAL FEVER (MEDITEMP)?

THERMOMETER, DIGITAL FEVER (MEDITEMP) is a medical device that received FDA 510(k) clearance on 1976-07-20. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K760118.

When did THERMOMETER, DIGITAL FEVER (MEDITEMP) receive FDA 510(k) clearance?

THERMOMETER, DIGITAL FEVER (MEDITEMP) received FDA 510(k) clearance on 1976-07-20, under 510(k) number K760118.

Who is the listed applicant for THERMOMETER, DIGITAL FEVER (MEDITEMP)?

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

What is the FDA product code for THERMOMETER, DIGITAL FEVER (MEDITEMP)?

The FDA product code for THERMOMETER, DIGITAL FEVER (MEDITEMP) is FLL.

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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.