510(k) K810738

GOODE MAGNETIC NASAL SPLINT by Xomed, Inc. — Product Code EPP

K810738 is an FDA 510(k) premarket notification submitted by Xomed, Inc. for the device "GOODE MAGNETIC NASAL SPLINT". The FDA issued a decision of Substantially Equivalent on March 31, 1981. The device falls under product code EPP (Splint, Nasal), a Class I device regulated under 21 CFR 874.5800. Xomed, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 31, 1981
Date Received
March 18, 1981
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Splint, Nasal
Device Class
Class I
Regulation Number
874.5800
Review Panel
EN
Submission Type