510(k) K894788
K894788 is an FDA 510(k) premarket notification submitted by M.D. Intl., Inc. for the device "DMI SERIES 90 EXAMINATION TABLE". The FDA issued a decision of Substantially Equivalent on September 8, 1989. The device falls under product code KMN (Chair And Table, Medical), a Class I device regulated under 21 CFR 880.6140. M.D. Intl., Inc. has at least 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 8, 1989
- Date Received
- July 28, 1989
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Chair And Table, Medical
- Device Class
- Class I
- Regulation Number
- 880.6140
- Review Panel
- HO
- Submission Type