510(k) K852202

STRUNG NEURO SPONGE PATTIES, X-RAY OPAGUE by Ormed Mfg., Inc. — Product Code EFQ

K852202 is an FDA 510(k) premarket notification submitted by Ormed Mfg., Inc. for the device "STRUNG NEURO SPONGE PATTIES, X-RAY OPAGUE". The FDA issued a decision of Substantially Equivalent on June 26, 1985. 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
June 26, 1985
Date Received
May 21, 1985
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