THUMPER

Pump, Infusion

BLOCK MEDICAL, INC.

The following data is part of a premarket notification filed by Block Medical, Inc. with the FDA for Thumper.

Pre-market Notification Details

• Device ID: K914854
• 510k Number: K914854
• Device Name: THUMPER
• Classification: Pump, Infusion
• Applicant: BLOCK MEDICAL, INC. 5957 LANDAU COURT Carlsbad, CA 92008
• Contact: Ian Kennedy
• Correspondent: Ian Kennedy; BLOCK MEDICAL, INC. 5957 LANDAU COURT Carlsbad, CA 92008
• Product Code: FRN
• CFR Regulation Number: 880.5725 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1991-10-28
• Decision Date: 1992-01-24