510(k) K915279
K915279 is an FDA 510(k) premarket notification submitted by Neoprobe Corp. for the device "NEOPROBE PORTABLE RADIOSCOPE DETECTOR". The FDA issued a decision of Substantially Equivalent on June 10, 1992. The device falls under product code IZD (Probe, Uptake, Nuclear), a Class I device regulated under 21 CFR 892.1320. Neoprobe Corp. has at least 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 10, 1992
- Date Received
- November 25, 1991
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Probe, Uptake, Nuclear
- Device Class
- Class I
- Regulation Number
- 892.1320
- Review Panel
- RA
- Submission Type