510(k) K801622

ADEL MEDICAL BIRTHING BED, MOD. LD-400 by Adel Medical , Ltd. — Product Code KNC

K801622 is an FDA 510(k) premarket notification submitted by Adel Medical , Ltd. for the device "ADEL MEDICAL BIRTHING BED, MOD. LD-400". The FDA issued a decision of Substantially Equivalent on August 14, 1980. The device falls under product code KNC (Table, Obstetric (And Accessories)), a Class II device regulated under 21 CFR 884.4900. Adel Medical , Ltd. has at least 7 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 14, 1980
Date Received
July 15, 1980
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Table, Obstetric (And Accessories)
Device Class
Class II
Regulation Number
884.4900
Review Panel
OB
Submission Type