510(k) K873831

EAR AND EYE SPONGES by Ormed Mfg., Inc. — Product Code EFQ

K873831 is an FDA 510(k) premarket notification submitted by Ormed Mfg., Inc. for the device "EAR AND EYE SPONGES". The FDA issued a decision of Substantially Equivalent on October 5, 1987. The device falls under product code EFQ (Gauze/Sponge, Internal), a Class U device. Ormed Mfg., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 5, 1987
Date Received
September 21, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Gauze/Sponge, Internal
Device Class
Class U
Regulation Number
Review Panel
SU
Submission Type