510(k) K862674

PHOTON ELITE/AUTOMATED RANDOM ACCESS IM/CH SYSTEM by Hybritech, Inc. — Product Code JZT

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