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FDA 510(k)

MODEL 90P PORTABLE MEDICAL DIAGNOSTIC X-RAY

K-Number: K934700 · 1994-03-16

ApplicantTempo Technology, Inc.
Decision Date1994-03-16
Product CodeOXO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODEL 90P PORTABLE MEDICAL DIAGNOSTIC X-RAY is the device name listed in this FDA 510(k) record. The listed applicant is Tempo Technology, Inc.. It received FDA 510(k) clearance on 1994-03-16 under 510(k) number K934700. The device is classified under product code OXO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 90P PORTABLE MEDICAL DIAGNOSTIC X-RAY?

MODEL 90P PORTABLE MEDICAL DIAGNOSTIC X-RAY is a medical device that received FDA 510(k) clearance on 1994-03-16. The listed applicant is Tempo Technology, Inc.. The 510(k) number is K934700.

When did MODEL 90P PORTABLE MEDICAL DIAGNOSTIC X-RAY receive FDA 510(k) clearance?

MODEL 90P PORTABLE MEDICAL DIAGNOSTIC X-RAY received FDA 510(k) clearance on 1994-03-16, under 510(k) number K934700.

Who is the listed applicant for MODEL 90P PORTABLE MEDICAL DIAGNOSTIC X-RAY?

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

What is the FDA product code for MODEL 90P PORTABLE MEDICAL DIAGNOSTIC X-RAY?

The FDA product code for MODEL 90P PORTABLE MEDICAL DIAGNOSTIC X-RAY is OXO.

Related Clinical Trials

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.

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Other records listing Tempo Technology, Inc. as applicant

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.

K963220TEMPRA COLD PACK, REORDER NO. TC150K896963TRIMODE SP DENTAL INTRA ORAL X-RAY

Related Devices (Code: OXO)

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.

K253296Digital C-ARM with 3DAllengers Medical Systems LimitedK252579Orthoscan TAU MVP Mini C-Arm SystemZiehm-Orthoscan, Inc.K253269OEC One CFDGe Hualun Medical Systems Co. , Ltd.K251004Dual-Mode Mobile C-Arm (Geelin500A, Geelin500M)Hefei Chimed Intelligent Machine Co., Ltd.K250587Orthoscan TAU Mini C-ArmZiehm-Orthoscan, Inc.K243452Orthoscan VERSA Mini C-ArmZiehm-Orthoscan, 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.

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