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FDA 510(k)

TEMPA-DOT CLINICAL THERMOMETER SHEATH

K-Number: K881286 · 1988-06-08

ApplicantPymah Corp.
Decision Date1988-06-08
Product CodeFQZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TEMPA-DOT CLINICAL THERMOMETER SHEATH is the device name listed in this FDA 510(k) record. The listed applicant is Pymah Corp.. It received FDA 510(k) clearance on 1988-06-08 under 510(k) number K881286. The device is classified under product code FQZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEMPA-DOT CLINICAL THERMOMETER SHEATH?

TEMPA-DOT CLINICAL THERMOMETER SHEATH is a medical device that received FDA 510(k) clearance on 1988-06-08. The listed applicant is Pymah Corp.. The 510(k) number is K881286.

When did TEMPA-DOT CLINICAL THERMOMETER SHEATH receive FDA 510(k) clearance?

TEMPA-DOT CLINICAL THERMOMETER SHEATH received FDA 510(k) clearance on 1988-06-08, under 510(k) number K881286.

Who is the listed applicant for TEMPA-DOT CLINICAL THERMOMETER SHEATH?

The FDA 510(k) record lists Pymah Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TEMPA-DOT CLINICAL THERMOMETER SHEATH?

The FDA product code for TEMPA-DOT CLINICAL THERMOMETER SHEATH is FQZ.

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Other records listing Pymah Corp. as applicant

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Related Devices (Code: FQZ)

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.

K110305CRY-ACTRACKERCAMBrymill Cryogenic CystemsK963049STERI-AID KITSteri-Aid, Inc.K946046DEROYAL TECHNOLOGICES, INC. LIQUID CRYSTAL SKIN TEMPERATURE STRIPDeroyal Critical Care, Div. Deroyal TechnologiesK894893POINT CHECKER COLOR STRIP THERMOMETERKyowa Medex Co., Ltd.K884612FRANKLIN COLLECTOR(R)Franklin Diagnostics, Inc.K863181HEALTHCHECK THERM-STRIPHealthcheck Corp.

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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