510(k) K801622
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