510(k) K894687

DYNATECH MR 5000, CATALOG #011-976-0600 by Dynatech Laboratories, Inc. — Product Code JJQ

K894687 is an FDA 510(k) premarket notification submitted by Dynatech Laboratories, Inc. for the device "DYNATECH MR 5000, CATALOG #011-976-0600". The FDA issued a decision of Substantially Equivalent on August 31, 1989. The device falls under product code JJQ (Colorimeter, Photometer, Spectrophotometer For Clinical Use), a Class I device regulated under 21 CFR 862.2300. Dynatech Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 31, 1989
Date Received
July 25, 1989
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