510(k) K850079

NOW HOME PREGN. TEST KIT ENZYME IMMUNOASSAY HCG by Bioclinical Systems, Inc. — Product Code LCX

K850079 is an FDA 510(k) premarket notification submitted by Bioclinical Systems, Inc. for the device "NOW HOME PREGN. TEST KIT ENZYME IMMUNOASSAY HCG". The FDA issued a decision of Substantially Equivalent on March 5, 1985. The device falls under product code LCX (Kit, Test, Pregnancy, Hcg, Over The Counter), a Class II device regulated under 21 CFR 862.1155. Bioclinical Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 5, 1985
Date Received
January 10, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Kit, Test, Pregnancy, Hcg, Over The Counter
Device Class
Class II
Regulation Number
862.1155
Review Panel
CH
Submission Type