510(k) K915161

AUGUSTINE FIBEROPTIC LARYNGOSCOPE by Augustine Medical, Inc. — Product Code CCW

K915161 is an FDA 510(k) premarket notification submitted by Augustine Medical, Inc. for the device "AUGUSTINE FIBEROPTIC LARYNGOSCOPE". The FDA issued a decision of Substantially Equivalent on May 29, 1992. 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
May 29, 1992
Date Received
November 14, 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