510(k) K884073

LARYNGOSCOPE BLADE (ROBERTSHAW STYLE) by Eastmed Enterprises, Inc. — Product Code CCW

K884073 is an FDA 510(k) premarket notification submitted by Eastmed Enterprises, Inc. for the device "LARYNGOSCOPE BLADE (ROBERTSHAW STYLE)". The FDA issued a decision of Substantially Equivalent on October 13, 1988. The device falls under product code CCW (Laryngoscope, Rigid), a Class I device regulated under 21 CFR 868.5540. Eastmed Enterprises, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 13, 1988
Date Received
September 27, 1988
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