510(k) K862674
K862674 is an FDA 510(k) premarket notification submitted by Hybritech, Inc. for the device "PHOTON ELITE/AUTOMATED RANDOM ACCESS IM/CH SYSTEM". The FDA issued a decision of Substantially Equivalent on August 15, 1986. The device falls under product code JZT (Fluorometer), a Class I device regulated under 21 CFR 866.4520. Hybritech, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 15, 1986
- Date Received
- July 14, 1986
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Fluorometer
- Device Class
- Class I
- Regulation Number
- 866.4520
- Review Panel
- IM
- Submission Type