VO RESPIRATORY PNEUMOTACHOGRAPH

Pneumotachometer

RESEARCH DEVELOPMENT CORP.

The following data is part of a premarket notification filed by Research Development Corp. with the FDA for Vo Respiratory Pneumotachograph.

Pre-market Notification Details

• Device ID: K770061
• 510k Number: K770061
• Device Name: VO RESPIRATORY PNEUMOTACHOGRAPH
• Classification: Pneumotachometer
• Applicant: RESEARCH DEVELOPMENT CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050
• Product Code: JAX
• CFR Regulation Number: 868.2550 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1977-01-11
• Decision Date: 1977-01-14

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
00850008733048	K770061	000