510(k) K943972
K943972 is an FDA 510(k) premarket notification submitted by Progressive Electrical Therapeutics for the device "EURO TECH DIAMOND CHIROPRACTIC TABLE". The FDA issued a decision of Substantially Equivalent on October 11, 1994. The device falls under product code INQ (Table, Powered), a Class I device regulated under 21 CFR 890.3760. Progressive Electrical Therapeutics has at least 9 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 11, 1994
- Date Received
- August 15, 1994
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Table, Powered
- Device Class
- Class I
- Regulation Number
- 890.3760
- Review Panel
- PM
- Submission Type