Atlas FDA

TARGET READER

FDA 510(k) clearance K885254 · decided 1989-01-27

Clearance details

K-number
K885254
Device name
TARGET READER
Applicant
V-Tech, Inc.
Decision
Substantially Equivalent
Date received
1988-12-23
Decision date
1989-01-27
Days to decision
35 days
Clearance type
Traditional
Product code
JQT
Device class
1
Regulation number
862.2400
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
Pomona, CA, 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
ASIMANAGER - AT (K111356)Arlington Scientific, Inc.2011-11-09
ISOSCAN (K944185)Isolab, Inc.1994-11-17
MODEL 795 FLUOROMETER/DENSITOMETER (K915332)Ciba Corning Diagnostics Corp.1992-02-18
ELECTROPHORESIS DATA CENTER (EDC) (K860645)Helena Laboratories1986-12-17
ICON READER (K862956)Hybritech, Inc.1986-08-19
APOLLO DENSITOMETER (K853734)Astral Medical Systems1985-09-25
ELECTROPHORESIS APPARATUS, FOR CLINICAL USE 160,18 (K851154)Astral Medical Systems1985-05-13
CORNING 780 FLUOROMETER/DENSITOMETER (K850617)Corning Medical & Scientific1985-03-12
GLEMAN ACD-2020 AUTOMATIC COMPUTING DENSITOMETER (K850260)Gelman Sciences, Inc.1985-02-27
ELVI 146 SEROSCAN (K842313)Logos Scientific, Inc.1984-09-10
ELVI 165 PROTEO SEROSKOP (K842056)Logos Scientific, Inc.1984-06-22
710 FLUOROMETER/DENSITOMETER (K810619)Corning Medical & Scientific1981-03-27

Recalls involving this device

No recalls on record reference this clearance.