Atlas FDA

ELECTR-TRANSBLOTTER

FDA 510(k) clearance K882344 · decided 1989-01-13

Clearance details

K-number
K882344
Device name
ELECTR-TRANSBLOTTER
Applicant
The W.E.P. Co.
Decision
Substantially Equivalent
Date received
1988-06-07
Decision date
1989-01-13
Days to decision
220 days
Clearance type
Traditional
Product code
JJN
Device class
1
Regulation number
862.2485
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
Seattle, WA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
POWER SUPPLY (K924021)The Binding Site, Ltd.1993-01-28
ELECTROPHORESIS TANK (K924020)The Binding Site, Ltd.1992-12-28
REP SP ELECTROPHORESIS SYSTEM CAT NO. 3170 (K881852)Helena Laboratories1988-07-08
HELENA REP GEL PROCESSOR (K882163)Helena Laboratories1988-06-20
RAPID ELECTROPHORESIS SYSTEM (REP) (K873352)Helena Laboratories1987-09-08
STAVIP 3000 (K864436)Roseburg SA1987-03-16
ELECTROPHORESIS WORK CENTER (EWC) (K861414)Helena Laboratories1986-08-26
ISOGEL AGAROSE (K841407)Fmc Corp.1985-07-16
EUROCHIMA SERUM PROTEIN ELECTROPHORESIS METHOD (K844710)Logos Scientific, Inc.1985-01-07
OPTIPHOR-10 (K842560)Gelman Sciences, Inc.1984-08-10
OPTICLEAR (K842485)Gelman Sciences, Inc.1984-08-10
ELVI 70 SAFETY CHAMBER (K841804)Logos Scientific, Inc.1984-05-31

Recalls involving this device

No recalls on record reference this clearance.