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FDA 510(k)

TARRY MEDICAL TEMPERATURE PROBES

K-Number: K071977 · 2008-05-23

ApplicantTarry Medical Products, Inc.
Decision Date2008-05-23
Product CodeFMZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TARRY MEDICAL TEMPERATURE PROBES is the device name listed in this FDA 510(k) record. The listed applicant is Tarry Medical Products, Inc.. It received FDA 510(k) clearance on 2008-05-23 under 510(k) number K071977. The device is classified under product code FMZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TARRY MEDICAL TEMPERATURE PROBES?

TARRY MEDICAL TEMPERATURE PROBES is a medical device that received FDA 510(k) clearance on 2008-05-23. The listed applicant is Tarry Medical Products, Inc.. The 510(k) number is K071977.

When did TARRY MEDICAL TEMPERATURE PROBES receive FDA 510(k) clearance?

TARRY MEDICAL TEMPERATURE PROBES received FDA 510(k) clearance on 2008-05-23, under 510(k) number K071977.

Who is the listed applicant for TARRY MEDICAL TEMPERATURE PROBES?

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

What is the FDA product code for TARRY MEDICAL TEMPERATURE PROBES?

The FDA product code for TARRY MEDICAL TEMPERATURE PROBES is FMZ.

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Related Devices (Code: FMZ)

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.

K260326Giraffe™ OmniBed™ Carestation (CS1); Giraffe™ Incubator Carestation (CS1)Datex-Ohmeda, Inc.K251619Babyleo TN500Drägerwerk AG & Co. KGaAK251663Giraffe OmniBed Carestation (CS1); Giraffe Incubator Carestation (CS1)Datex-Ohmeda, Inc.K243437mOm Essential Incubator (ME1)Mom Incubators LimitedK213553Giraffe Incubator Carestation CS1Datex Ohmeda, Inc.K190494Infant IncubatorNingbo David Medical Device Co., Ltd.

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.

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