Atlas FDA

SPECTRUM-10

FDA 510(k) clearance K831655 · decided 1983-06-17

Clearance details

K-number
K831655
Device name
SPECTRUM-10
Applicant
Austin Biological Laboratories
Decision
Substantially Equivalent
Date received
1983-05-23
Decision date
1983-06-17
Days to decision
25 days
Clearance type
Traditional
Product code
JSZ
Device class
1
Regulation number
866.2660
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.