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510(k) K772380

Device
Farrior Oval Speculum
Applicant
EDWARD WECK, INC.
510(k) number
K772380
Product code
EPY
Decision
Substantially Equivalent (SESE)
Decision date
1978-01-17
Date received
1977-12-27
Regulation
878.1800
Classification name
Speculum, Ent
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
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 EPY#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K950086PEDIA PALS, INCORPORATEDPedia Pals, Inc.1995-02-07
K925754ECONOMRudolf Riester GmbH & Co. KG1993-10-08
K853588FIBRELIGHT NASAL SPECULADowns Surgical , Ltd.1985-12-18
K834189JAKOBI SURG. INSTRUMENTS #7 44/47Imm Enterprises , Ltd.1984-03-06
K822370UNIVERSAL SPECULUM HOLDERTreace Medical, Inc.1982-09-09
K822373EAR SURGERY SPECULUMTreace Medical, Inc.1982-09-09
K822164EAR SPECULIKelleher Corp.1982-08-11
K791123EAR AND NOSE SPECULAXomed, Inc.1979-07-10
K780723OTOSCOPE SPECULAAbco Dealers, Inc.1978-05-09
K772370BARRAQUER OVAL SPECULUM-VARIOUS SIZESEdward Weck, Inc.1978-01-17
K772385THIN-BLADED NASAL SPECULUMEdward Weck, Inc.1978-01-17