FDA 510(k)

EXAC-TEMP & CLINI-TEMP TYMPANIC & MYOCARDIAL PROBE

K-Number: K925792 · 1994-04-08

Decision Date1994-04-08

Product CodeFLL

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

EXAC-TEMP & CLINI-TEMP TYMPANIC & MYOCARDIAL PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Deroyal Industries, Inc.. It received FDA 510(k) clearance on 1994-04-08 under 510(k) number K925792. 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 EXAC-TEMP & CLINI-TEMP TYMPANIC & MYOCARDIAL PROBE?

EXAC-TEMP & CLINI-TEMP TYMPANIC & MYOCARDIAL PROBE is a medical device that received FDA 510(k) clearance on 1994-04-08. The listed applicant is Deroyal Industries, Inc.. The 510(k) number is K925792.

When did EXAC-TEMP & CLINI-TEMP TYMPANIC & MYOCARDIAL PROBE receive FDA 510(k) clearance?

EXAC-TEMP & CLINI-TEMP TYMPANIC & MYOCARDIAL PROBE received FDA 510(k) clearance on 1994-04-08, under 510(k) number K925792.

Who is the listed applicant for EXAC-TEMP & CLINI-TEMP TYMPANIC & MYOCARDIAL PROBE?

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

What is the FDA product code for EXAC-TEMP & CLINI-TEMP TYMPANIC & MYOCARDIAL PROBE?

The FDA product code for EXAC-TEMP & CLINI-TEMP TYMPANIC & MYOCARDIAL PROBE is FLL.

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Related Devices (Code: 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.