510(k) K760906

Device
Monomer Vapor Containment System
Applicant
HOWMEDICA CORP.
510(k) number
K760906
Product code
JDY
Decision
Substantially Equivalent (SESE)
Decision date
1976-11-11
Date received
1976-10-26
Regulation
888.4220
Classification name
Evacuator, Vapor, Cement Monomer
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
1
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 JDY#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K902167CONTAIN(TM) LASER PLUME FILTERArbor Technologies, Inc.1991-01-04
K902056LASER TRAP 100 LASER PLUME SMOKE EVACUATION FILTERHollister, Inc.1990-10-30
K862509CHARCOAL LASER SMOKE FILTER CATALOG NO. 901103-000Lifestream Int'L, Inc.1986-07-23
K810542CEMENT FUME EVACUATOR TANK & FILTERWalgen Medical Innoventions1981-03-13
K790877BIOVAC: LFA LASER FUME (SMOKE) EVACUATIOStackhouse Assoc.1979-05-23
K780202MONOMER EVACUATION SYSTEMMedishield, Inc.1978-02-21
K770690MASK, VAPOR, MONOMERHowmedica Corp.1977-07-21