510(k) K943972

EURO TECH DIAMOND CHIROPRACTIC TABLE by Progressive Electrical Therapeutics — Product Code INQ

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