510(k) K952505
K952505 is an FDA 510(k) premarket notification submitted by Nichols Institute for the device "INSULIN-LIKE GROWTH FACTOR I (IGF-I), IMMUNORADIOMETERIC ASSAY (IRMA)". The FDA issued a decision of Substantially Equivalent on July 3, 1995. The device falls under product code CFL (Radioimmunoassay, Human Growth Hormone), a Class I device regulated under 21 CFR 862.1370. Nichols Institute has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 3, 1995
- Date Received
- May 31, 1995
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Radioimmunoassay, Human Growth Hormone
- Device Class
- Class I
- Regulation Number
- 862.1370
- Review Panel
- CH
- Submission Type