FDA.reportPublic FDA data

510(k) K760851

Device
CONVERSE ALTAR RETRACTOR
Applicant
V. Mueller O.V. Baxter Healthcare Corp.
510(k) number
K760851
Product code
KAL
Decision
Substantially Equivalent (SESE)
Decision date
1977-03-10
Date received
1976-10-15
Regulation
874.4420
Classification name
Retractor, Ent
Medical specialty
Ear, Nose, Throat
Review panel
Ear, Nose, Throat
Device class
1
Clearance type
Traditional
Third party reviewed
N

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 KAL#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K870758SMALL MASTOID RETRACTORTreace Medical, Inc.1987-03-04
K833604ADJUSTABLE FORK RETRACTORMicrotek Medical, Inc.1984-01-03
K772381RING HANDLE & RETRACTORSEdward Weck, Inc.1978-01-17
K772392ALLPORT MASTOID RETRACTORSEdward Weck, Inc.1978-01-17