Atlas FDA

SAMPLE IDENTIFICATION STATION MODEL 38010

FDA 510(k) clearance K884269 · decided 1989-01-09

Clearance details

K-number
K884269
Device name
SAMPLE IDENTIFICATION STATION MODEL 38010
Applicant
Icn Micromedic Systems
Decision
Substantially Equivalent
Date received
1988-10-11
Decision date
1989-01-09
Days to decision
90 days
Clearance type
Traditional
Product code
JJJ
Device class
1
Regulation number
862.2320
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
Horsham, PA, US
Third-party review
No
Expedited review
No

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RecordFirmDate
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SOURCERER (K894902)Oakfield Instruments, Ltd.1989-10-17
SOURCERER (K884091)John Caunt Scientific , Ltd.1989-02-02
1205 BETAPLATE LIQUID SCINTILLATION COUNTER (K874094)Lkb Instruments, Inc.1987-11-04
ISO-DATA 500 SERIES GAMMA COUNTER (K872430)Iso-Data, Inc.1987-08-21
ISO-DATA 100 SERIES GAMMA COUNTER (K872429)Iso-Data, Inc.1987-08-21
BERTHOLD LB 2103,2104-XT/PC/AT,951G GAMMA COUNTERS (K870115)Berthold Analytical Instruments, Inc.1987-03-31
TAURUS (TM) AUTOMATIC LIQUID SCINTILLATION COUNTER (K862206)Micromedic Systems1986-08-04

Recalls involving this device

No recalls on record reference this clearance.