LOCKBOX

Pump, Infusion

PHARMACIA DELTEC, INC.

The following data is part of a premarket notification filed by Pharmacia Deltec, Inc. with the FDA for Lockbox.

Pre-market Notification Details

• Device ID: K900888
• 510k Number: K900888
• Device Name: LOCKBOX
• Classification: Pump, Infusion
• Applicant: PHARMACIA DELTEC, INC. 1265 GREY FOX RD. St. Paul, MN 55112
• Contact: Lisa J Stone
• Correspondent: Lisa J Stone; PHARMACIA DELTEC, INC. 1265 GREY FOX RD. St. Paul, MN 55112
• Product Code: FRN
• CFR Regulation Number: 880.5725 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1990-02-26
• Decision Date: 1990-05-15

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
10610586026966	K900888	000
10610586026959	K900888	000
10610586026942	K900888	000
10610586026928	K900888	000
10610586028113	K900888	000
10610586028090	K900888	000