FDA 510(k)

EQUILIBRIUM RADIONUCLIDE ANGIOCARDIORAPHY ANALYSIS

K-Number: K925186 · 1993-01-12

ApplicantStrichman Medical Equipment, Inc.

Decision Date1993-01-12

Product CodeKPS

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

EQUILIBRIUM RADIONUCLIDE ANGIOCARDIORAPHY ANALYSIS is the device name listed in this FDA 510(k) record. The listed applicant is Strichman Medical Equipment, Inc.. It received FDA 510(k) clearance on 1993-01-12 under 510(k) number K925186. The device is classified under product code KPS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EQUILIBRIUM RADIONUCLIDE ANGIOCARDIORAPHY ANALYSIS?

EQUILIBRIUM RADIONUCLIDE ANGIOCARDIORAPHY ANALYSIS is a medical device that received FDA 510(k) clearance on 1993-01-12. The listed applicant is Strichman Medical Equipment, Inc.. The 510(k) number is K925186.

When did EQUILIBRIUM RADIONUCLIDE ANGIOCARDIORAPHY ANALYSIS receive FDA 510(k) clearance?

EQUILIBRIUM RADIONUCLIDE ANGIOCARDIORAPHY ANALYSIS received FDA 510(k) clearance on 1993-01-12, under 510(k) number K925186.

Who is the listed applicant for EQUILIBRIUM RADIONUCLIDE ANGIOCARDIORAPHY ANALYSIS?

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

What is the FDA product code for EQUILIBRIUM RADIONUCLIDE ANGIOCARDIORAPHY ANALYSIS?

The FDA product code for EQUILIBRIUM RADIONUCLIDE ANGIOCARDIORAPHY ANALYSIS is KPS.

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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.