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FDA 510(k)

TEMPO III

K-Number: K981509 · 1998-07-10

ApplicantMedical Products, Inc.
Decision Date1998-07-10
Product CodeLGZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TEMPO III is the device name listed in this FDA 510(k) record. The listed applicant is Medical Products, Inc.. It received FDA 510(k) clearance on 1998-07-10 under 510(k) number K981509. The device is classified under product code LGZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEMPO III?

TEMPO III is a medical device that received FDA 510(k) clearance on 1998-07-10. The listed applicant is Medical Products, Inc.. The 510(k) number is K981509.

When did TEMPO III receive FDA 510(k) clearance?

TEMPO III received FDA 510(k) clearance on 1998-07-10, under 510(k) number K981509.

Who is the listed applicant for TEMPO III?

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

What is the FDA product code for TEMPO III?

The FDA product code for TEMPO III is LGZ.

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Related Devices (Code: LGZ)

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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.

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