510(k) K912318
K912318 is an FDA 510(k) premarket notification submitted by Serono-Baker Diagnostics, Inc. for the device "ESTRADIOL SEROZYME ENZYME IMMUNO (MAG SOLID-PHASE)". The FDA issued a decision of Substantially Equivalent on July 25, 1991. The device falls under product code CHP (Radioimmunoassay, Estradiol), a Class I device regulated under 21 CFR 862.1260. Serono-Baker Diagnostics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 25, 1991
- Date Received
- May 24, 1991
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Radioimmunoassay, Estradiol
- Device Class
- Class I
- Regulation Number
- 862.1260
- Review Panel
- CH
- Submission Type