HANDI-MOVE

Transport, Patient, Powered

T.F. HERCEG, INC.

The following data is part of a premarket notification filed by T.f. Herceg, Inc. with the FDA for Handi-move.

Pre-market Notification Details

• Device ID: K854461
• 510k Number: K854461
• Device Name: HANDI-MOVE
• Classification: Transport, Patient, Powered
• Applicant: T.F. HERCEG, INC. 33 RECTOR ST. New York, NY 10006
• Contact: Thomas F Herceh
• Correspondent: Thomas F Herceh; T.F. HERCEG, INC. 33 RECTOR ST. New York, NY 10006
• Product Code: ILK
• CFR Regulation Number: 890.5150 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1985-11-06
• Decision Date: 1986-03-14