510(k) K972364

UNICAP PHADIATOP by Pharmacia, Inc. — Product Code DHB

K972364 is an FDA 510(k) premarket notification submitted by Pharmacia, Inc. for the device "UNICAP PHADIATOP". The FDA issued a decision of Substantially Equivalent on September 4, 1997. The device falls under product code DHB (System, Test, Radioallergosorbent (Rast) Immunological), a Class II device regulated under 21 CFR 866.5750. Pharmacia, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 4, 1997
Date Received
June 25, 1997
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Test, Radioallergosorbent (Rast) Immunological
Device Class
Class II
Regulation Number
866.5750
Review Panel
IM
Submission Type