Radioassay, Angiotensin Converting Enzyme

Device Code: 594

Product Code(s): KQN

Device Classification Information

• Device Type ID: 594
• Device Name: Radioassay, Angiotensin Converting Enzyme
• Regulation Description: Angiotensin Converting Enzyme (A.C.E.) 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) Exempt
• CFR Regulation Number: 862.1090 [🔎]
• FDA Device Classification: Class 2 Medical Device
• Product Code: KQN
• 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: 594
• Device: Radioassay, Angiotensin Converting Enzyme
• Product Code: KQN
• FDA Device Classification: Class 2 Medical Device
• Regulation Description: Angiotensin Converting Enzyme (A.C.E.) Test System.
• CFR Regulation Number: 862.1090 [🔎]

TPLC Last Update: 2019-04-02 19:37:03