510(k) K980796

TERUMO ALLERGY SYRINGE by Terumo Corp. — Product Code FMF

K980796 is an FDA 510(k) premarket notification submitted by Terumo Corp. for the device "TERUMO ALLERGY SYRINGE". The FDA issued a decision of Substantially Equivalent on April 2, 1998. The device falls under product code FMF (Syringe, Piston), a Class II device regulated under 21 CFR 880.5860. Terumo Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 2, 1998
Date Received
March 2, 1998
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Syringe, Piston
Device Class
Class II
Regulation Number
880.5860
Review Panel
HO
Submission Type