Cleared Traditional

K960029 - HYDRASYS AGAROSE GEL ELECTROPHORESIS APPARATUS/HYDRAGEL 15,30 PROTEIN KIT
(FDA 510(k) Clearance)

Jul 1996
Decision
197d
Days
Class 1
Risk

K960029 is an FDA 510(k) clearance for the HYDRASYS AGAROSE GEL ELECTROPHORESIS APPARATUS/HYDRAGEL 15,30 PROTEIN KIT. This device is classified as a Electrophoretic, Protein Fractionation (Class I - General Controls, product code CEF).

Submitted by Morax (Chelsea, US). The FDA issued a Cleared decision on July 17, 1996, 197 days after receiving the submission on January 2, 1996.

This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1630.

Submission Details

510(k) Number K960029 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 02, 1996
Decision Date July 17, 1996
Days to Decision 197 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary Statement

Device Classification

Product Code CEF — Electrophoretic, Protein Fractionation
Device Class Class I - General Controls
CFR Regulation 21 CFR 862.1630

Similar Devices — CEF Electrophoretic, Protein Fractionation

All 28
CAPILLARYS IMMUNOTYPING, CAPILLARYS 2 INSTRUMENT, IT/IF CONTROL, CAPILLARYS 2 FLEX PIERCING INSTRUMENT
K130500 · Sebia · Jul 2013
SPIFE
K972274 · Helena Laboratories · Oct 1997
REP SPE VIS-60/40 KIT
K973316 · Helena Laboratories · Oct 1997
BIO-RAD SERUM PROTEINS BY CAPILLARY ELECTROPHORESIS
K963018 · Bio-Rad · Jun 1997
REP 3 FLUR SPE-60 KIT
K964453 · Helena Laboratories · Dec 1996
HYDRAGEL PROTEIN(E) KIT
K951536 · Sebia · Jun 1995