510(k) K873831
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