510(k) K864932

'EXMOOR' CAWOOD NASAL SPLINTS by Exmoor Plastics , Ltd. — Product Code EPP

K864932 is an FDA 510(k) premarket notification submitted by Exmoor Plastics , Ltd. for the device "'EXMOOR' CAWOOD NASAL SPLINTS". The FDA issued a decision of Substantially Equivalent on March 4, 1987. The device falls under product code EPP (Splint, Nasal), a Class I device regulated under 21 CFR 874.5800. Exmoor Plastics , Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 4, 1987
Date Received
December 16, 1986
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