Atlas FDA

ATOMLIGHT (LIQUID SCINTILLATION SOLUTION

FDA 510(k) clearance K801245 · decided 1980-06-20

Clearance details

K-number
K801245
Device name
ATOMLIGHT (LIQUID SCINTILLATION SOLUTION
Applicant
New England Nuclear
Decision
Substantially Equivalent
Date received
1980-05-27
Decision date
1980-06-20
Days to decision
24 days
Clearance type
Traditional
Product code
JJJ
Device class
1
Regulation number
862.2320
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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RecordFirmDate
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ABBOTT VERTEX ANALYZER (K920559)Abbott Laboratories1992-03-19
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SOURCERER (K894902)Oakfield Instruments, Ltd.1989-10-17
SOURCERER (K884091)John Caunt Scientific , Ltd.1989-02-02
SAMPLE IDENTIFICATION STATION MODEL 38010 (K884269)Icn Micromedic Systems1989-01-09
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

Recalls involving this device

No recalls on record reference this clearance.