MODEL M1032A VUELINK INTERFACE PLUG-IN MODULE

Oximeter

HEWLETT-PACKARD CO.

The following data is part of a premarket notification filed by Hewlett-packard Co. with the FDA for Model M1032a Vuelink Interface Plug-in Module.

Pre-market Notification Details

• Device ID: K923682
• 510k Number: K923682
• Device Name: MODEL M1032A VUELINK INTERFACE PLUG-IN MODULE
• Classification: Oximeter
• Applicant: HEWLETT-PACKARD CO. SCHUCKARDSTRABE 4 7030 BOBLINGEN Germany, DE
• Contact: Gerhard Lenke
• Correspondent: Gerhard Lenke; HEWLETT-PACKARD CO. SCHUCKARDSTRABE 4 7030 BOBLINGEN Germany, DE
• Product Code: DQA
• CFR Regulation Number: 870.2700 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1992-07-23
• Decision Date: 1992-09-28

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
00884838021099	K923682	000