510(k) K931635
K931635 is an FDA 510(k) premarket notification submitted by Med Mart, Inc. for the device "TREATMENT TABLES, MANUALLY ACTIVATED". The FDA issued a decision of Substantially Equivalent on July 21, 1993. The device falls under product code INW (Table, Mechanical), a Class I device regulated under 21 CFR 890.3750. Med Mart, Inc. has at least 4 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 21, 1993
- Date Received
- April 1, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Table, Mechanical
- Device Class
- Class I
- Regulation Number
- 890.3750
- Review Panel
- PM
- Submission Type