510(k) K882884

STORZ INFUSION CANNULA by Storz Instrument Co. — Product Code HMX

K882884 is an FDA 510(k) premarket notification submitted by Storz Instrument Co. for the device "STORZ INFUSION CANNULA". The FDA issued a decision of Substantially Equivalent on August 4, 1988. The device falls under product code HMX (Cannula, Ophthalmic), a Class I device regulated under 21 CFR 886.4350. Storz Instrument Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 4, 1988
Date Received
July 11, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Cannula, Ophthalmic
Device Class
Class I
Regulation Number
886.4350
Review Panel
OP
Submission Type