DeviceClearance

QUIKPAC-II ONE STEP PREGNANCY HOME TEST— 510(k) K912316

Substantially Equivalent

Syntron Bioresearch, Inc.

FDA 510(k) clearance K912316 for QUIKPAC-II ONE STEP PREGNANCY HOME TEST, Substantially Equivalent on 1991-07-24. Applicant: Syntron Bioresearch, Inc..

Clearance details

Applicant
Syntron Bioresearch, Inc.
Product code
Code LCX
Advisory panel
Clinical Chemistry
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Vista, CA, US
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