Apollo Gamma Camera System

FDA 510(k) K062298 · Adac Laboratories

Substantially Equivalent

510(k) numberK062298

Submission

Device name
Apollo Gamma Camera System
Applicant
Adac Laboratories
Milpitas, CA, US
Received
August 8, 2006
Decision date
August 23, 2006
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA
Third-party review
Yes

Official FDA 510(k) record

Device classification

Product code
KPS – System, Tomography, Computed, Emission
Device class
Class II (moderate risk)
Regulation
21 CFR 892.1200
Specialty
Radiology

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Questions and answers

When was Apollo Gamma Camera System cleared by the FDA?

Apollo Gamma Camera System (K062298) received a 510(k) decision of Substantially Equivalent on August 23, 2006, 15 days after the submission was received.

What is the product code of K062298?

The FDA product code is KPS – System, Tomography, Computed, Emission, a Class II (moderate risk) device regulated under 21 CFR 892.1200.