510(k) K934844

INTER TIP T by Microsurgical Technology, Inc. — Product Code HMX

K934844 is an FDA 510(k) premarket notification submitted by Microsurgical Technology, Inc. for the device "INTER TIP T". The FDA issued a decision of Substantially Equivalent on April 19, 1994. The device falls under product code HMX (Cannula, Ophthalmic), a Class I device regulated under 21 CFR 886.4350. Microsurgical Technology, Inc. has at least 8 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 19, 1994
Date Received
October 8, 1993
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