510(k) K930317

REP SPE HI-RES TEMPLATE SYSTEM, CAT 3276/3277/3278 by Helena Laboratories — Product Code CEF

K930317 is an FDA 510(k) premarket notification submitted by Helena Laboratories for the device "REP SPE HI-RES TEMPLATE SYSTEM, CAT 3276/3277/3278". The FDA issued a decision of Substantially Equivalent on August 3, 1993. The device falls under product code CEF (Electrophoretic, Protein Fractionation), a Class I device regulated under 21 CFR 862.1630. Helena Laboratories has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 3, 1993
Date Received
January 22, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Electrophoretic, Protein Fractionation
Device Class
Class I
Regulation Number
862.1630
Review Panel
CH
Submission Type