510(k) K923176

SURGICAL INSTRUMENT KIT, DISPOSABLE by Ulti-Med Intl., Inc. — Product Code KDD

K923176 is an FDA 510(k) premarket notification submitted by Ulti-Med Intl., Inc. for the device "SURGICAL INSTRUMENT KIT, DISPOSABLE". The FDA issued a decision of Substantially Equivalent on June 17, 1993. The device falls under product code KDD (Kit, Surgical Instrument, Disposable), a Class I device regulated under 21 CFR 878.4800. Ulti-Med Intl., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 17, 1993
Date Received
June 12, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Kit, Surgical Instrument, Disposable
Device Class
Class I
Regulation Number
878.4800
Review Panel
SU
Submission Type