Radioimmunoassay, Cyclic Gmp

Device Code: 305

Product Code(s): CGT

Device Classification Information

• Device Type ID: 305
• Device Name: Radioimmunoassay, Cyclic Gmp
• Regulation Description: Cyclic AMP Test System.
• Regulation Medical Specialty: Clinical Chemistry
• Review Panel: Clinical Chemistry
• Premarket Review: Office Of In Vitro Diagnostics And Radiological Health (OIR)
• Submission Type: 510(k)
• CFR Regulation Number: 862.1230 [🔎]
• FDA Device Classification: Class 2 Medical Device
• Product Code: CGT
• GMP Exempt: No
• Summary MR: Eligible
• Implanted Device: No
• Life Support Device: No
• Third Party Review: Eligible For Accredited Persons Expansion Pilot Program

Recognized Standards

Total Product Life Cycle

• Device Type ID: 305
• Device: Radioimmunoassay, Cyclic Gmp
• Product Code: CGT
• FDA Device Classification: Class 2 Medical Device
• Regulation Description: Cyclic AMP Test System.
• CFR Regulation Number: 862.1230 [🔎]

TPLC Last Update: 2019-04-02 19:32:29