510(k) K830983

AIRWAYS & NASOPHARYNGEAL TYPE by Medovations, Inc. — Product Code BTQ

K830983 is an FDA 510(k) premarket notification submitted by Medovations, Inc. for the device "AIRWAYS & NASOPHARYNGEAL TYPE". The FDA issued a decision of Substantially Equivalent on May 9, 1983. The device falls under product code BTQ (Airway, Nasopharyngeal), a Class I device regulated under 21 CFR 868.5100. Medovations, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 9, 1983
Date Received
March 29, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Airway, Nasopharyngeal
Device Class
Class I
Regulation Number
868.5100
Review Panel
AN
Submission Type