FDA 510(k)

E-Z TEMP II

K-Number: K934941 · 1994-07-27

Decision Date1994-07-27

Product CodeKPD

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

E-Z TEMP II is the device name listed in this FDA 510(k) record. The listed applicant is Seven C'S, Inc.. It received FDA 510(k) clearance on 1994-07-27 under 510(k) number K934941. The device is classified under product code KPD. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the E-Z TEMP II?

E-Z TEMP II is a medical device that received FDA 510(k) clearance on 1994-07-27. The listed applicant is Seven C'S, Inc.. The 510(k) number is K934941.

When did E-Z TEMP II receive FDA 510(k) clearance?

E-Z TEMP II received FDA 510(k) clearance on 1994-07-27, under 510(k) number K934941.

Who is the listed applicant for E-Z TEMP II?

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

What is the FDA product code for E-Z TEMP II?

The FDA product code for E-Z TEMP II is KPD.

Related Devices (Code: KPD)

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.

K903307TEMP MARQ TEMPERATURE TREND INDICATORMarquest Medical Products, Inc.K893803FEVER LINE AND FEVER LINE PLUSLiquid Crystal Sciences, Inc.K864853OMNI THERM TEMPERATURE MONITOROmni Therm, Inc.K850797TEMPALERT LIQUID CRYSTAL THERMOMETERMedical Frontiers, Inc.K841913TEMPTREND PEDS AXILLARY TEMP. INDICATORBiosynergy, Inc.K833904TEMPTREND IIBiosynergy, Inc.

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.