Atlas FDA

QUANTIMETRIX C-CLEAR(TM)

FDA 510(k) clearance K931523 · decided 1993-06-25

Clearance details

K-number
K931523
Device name
QUANTIMETRIX C-CLEAR(TM)
Applicant
Quantimetrix Corp.
Decision
Substantially Equivalent
Date received
1993-03-26
Decision date
1993-06-25
Days to decision
91 days
Clearance type
Traditional
Product code
JMA
Device class
1
Regulation number
862.1095
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
Hawthorne, 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
HELENA BIOSTRIP A (K830978)Helena Laboratories1983-05-13
URITEST 9, INLAB REAGENT STRIPS URINALY (K822709)Laprol Scientific, Inc.1983-01-28

Recalls involving this device

No recalls on record reference this clearance.