510(k) K873138

MICRO-READER II by Hyperion, Inc. — Product Code JJQ

K873138 is an FDA 510(k) premarket notification submitted by Hyperion, Inc. for the device "MICRO-READER II". The FDA issued a decision of Substantially Equivalent on September 14, 1987. The device falls under product code JJQ (Colorimeter, Photometer, Spectrophotometer For Clinical Use), a Class I device regulated under 21 CFR 862.2300. Hyperion, Inc. has at least 7 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 14, 1987
Date Received
August 10, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Colorimeter, Photometer, Spectrophotometer For Clinical Use
Device Class
Class I
Regulation Number
862.2300
Review Panel
CH
Submission Type