Antisera, Hai, Reovirus 1-3

Device Code: 3240

Product Code(s): GPY

Device Classification Information

• Device Type ID: 3240
• Device Name: Antisera, Hai, Reovirus 1-3
• Regulation Description: Reovirus Serological Reagents.
• Regulation Medical Specialty: Microbiology
• Review Panel: Microbiology
• Premarket Review: Office Of In Vitro Diagnostics And Radiological Health (OIR)
• Submission Type: 510(K) Exempt
• CFR Regulation Number: 866.3470 [🔎]
• FDA Device Classification: Class 1 Medical Device
• Product Code: GPY
• GMP Exempt: No
• Summary MR: Eligible
• Implanted Device: No
• Life Support Device: No
• Third Party Review: Not Third Party Eligible

Recognized Standards

Total Product Life Cycle

• Device Type ID: 3240
• Device: Antisera, Hai, Reovirus 1-3
• Product Code: GPY
• FDA Device Classification: Class 1 Medical Device
• Regulation Description: Reovirus Serological Reagents.
• CFR Regulation Number: 866.3470 [🔎]

TPLC Last Update: 2019-04-02 20:26:16