Atlas FDA

TENONE(TM) OPIATES CATALOG: VKSO1,4

FDA 510(k) clearance K902055 · decided 1990-07-10

Clearance details

K-number
K902055
Device name
TENONE(TM) OPIATES CATALOG: VKSO1,4
Applicant
Diagnostic Products Corp.
Decision
Substantially Equivalent
Date received
1990-05-07
Decision date
1990-07-10
Days to decision
64 days
Clearance type
Traditional
Product code
DDE
Device class
1
Regulation number
866.5200
Medical specialty
Immunology
Advisory committee
Immunology
Location
Los Angeles, 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
COAT-A-COUNT MORPHINE KIT & COMPONENTS (K823680)Diagnostic Products Corp.1983-01-05
EMIT URINE METHADONE ASSAY #3E319 (K820900)Syva Co.1982-04-26

Recalls involving this device

No recalls on record reference this clearance.