510(k) K943975

EURO TECH PLATINUM CHIROPRACTIC TABLE by Progressive Electrical Therapeutics — Product Code INW

K943975 is an FDA 510(k) premarket notification submitted by Progressive Electrical Therapeutics for the device "EURO TECH PLATINUM CHIROPRACTIC TABLE". The FDA issued a decision of Substantially Equivalent on September 29, 1994. The device falls under product code INW (Table, Mechanical), a Class I device regulated under 21 CFR 890.3750. Progressive Electrical Therapeutics has at least 9 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 29, 1994
Date Received
August 15, 1994
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