510(k) K914168

AUGUSTINE GUIDE KIT WITH GAUZE SPONGE by Augustine Medical, Inc. — Product Code CCW

K914168 is an FDA 510(k) premarket notification submitted by Augustine Medical, Inc. for the device "AUGUSTINE GUIDE KIT WITH GAUZE SPONGE". The FDA issued a decision of Substantially Equivalent on October 7, 1991. The device falls under product code CCW (Laryngoscope, Rigid), a Class I device regulated under 21 CFR 868.5540. Augustine Medical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 7, 1991
Date Received
September 17, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Laryngoscope, Rigid
Device Class
Class I
Regulation Number
868.5540
Review Panel
AN
Submission Type