510(k) K801070

SHERWOOD DISPOSABLE ENDOMETRIAL SAMPLES by Sherwood Medical Industries — Product Code HHK

K801070 is an FDA 510(k) premarket notification submitted by Sherwood Medical Industries for the device "SHERWOOD DISPOSABLE ENDOMETRIAL SAMPLES". The FDA issued a decision of Substantially Equivalent on July 21, 1980. The device falls under product code HHK (Curette, Suction, Endometrial (And Accessories)), a Class II device regulated under 21 CFR 884.1175. Sherwood Medical Industries has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 21, 1980
Date Received
May 6, 1980
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Curette, Suction, Endometrial (And Accessories)
Device Class
Class II
Regulation Number
884.1175
Review Panel
OB
Submission Type