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510(k) K770061

Device
VO RESPIRATORY PNEUMOTACHOGRAPH
Applicant
RESEARCH DEVELOPMENT CORP.
510(k) number
K770061
Product code
JAX  
Decision
Substantially Equivalent (SESE)
Decision date
1977-01-14
Date received
1977-01-11
Regulation
868.2550
Classification name
Pneumotachometer
Medical specialty
Anesthesiology
Review panel
Anesthesiology
Device class
2
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Address
803 N. Front St. Suite 3 Mchenry IL US 60050 60050

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code JAX  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K990962FLOSENSE, MODEL 29-8010Sdi Diagnostics, Inc.2000-01-07
K921178PTI-A, PTI-P, PTI-N DISPOSABLE PNEUMOTACHSMedical Associated Services, Inc.1992-08-26
K884464SPIROMETRICS MODEL 2200 SM200 FLOW SENSORSpirometrics, Inc.1989-01-19
K853085PAX METERPeace Medical, Inc.1985-09-03
K833265RESPIRATORY FLOW MODULEThoratec Laboratories Corp.1983-11-28
K812825FLO-COR IBiotrine Corp.1981-10-26
K791730RING-ORIFICE, TURBULENT FLOW PNEUMOTResearch Development Corp.1979-11-16

Legacy Summary#

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FDA Review#

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