FDA.reportPublic FDA data

510(k) K780407

Device
2c7125 Blow Bottle
Applicant
TRAVENOL LABORATORIES, S.A.
510(k) number
K780407
Product code
BYO
Decision
Substantially Equivalent (SESE)
Decision date
1978-04-10
Date received
1978-03-13
Regulation
868.5220
Classification name
Bottle, Blow
Medical specialty
Anesthesiology
Review panel
Anesthesiology
Device class
1
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Address
4221 Richmond Rd., NW Walker MI US 49534 49534

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code BYO#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K924541EPIDURAL MINIPACKConcord/Portex1993-07-09
K913527HYPERFREEKist Intl.1992-01-21
K780558BOTTLE BREATHING DEVICEB & F Medical Products, Inc.1978-05-26