510(k) K772139
K772139 is an FDA 510(k) premarket notification submitted by Geometric Data, Div. Smithkline Corp. for the device "RE-CELL SLIDE RECAP". The FDA issued a decision of Substantially Equivalent on January 5, 1978. The device falls under product code JOY (Device, Automated Cell-Locating), a Class II device regulated under 21 CFR 864.5260. Geometric Data, Div. Smithkline Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 5, 1978
- Date Received
- November 14, 1977
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Device, Automated Cell-Locating
- Device Class
- Class II
- Regulation Number
- 864.5260
- Review Panel
- HE
- Submission Type