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510(k) K772396

Device
ALLIGATOR CUP FORCEPS
Applicant
EDWARD WECK, INC.
510(k) number
K772396
Product code
KAE  
Decision
Substantially Equivalent (SESE)
Decision date
1978-01-17
Date received
1977-12-27
Regulation
874.4420
Classification name
Forceps, Ent
Medical specialty
Ear Nose & Throat
Review panel
Ear Nose & Throat
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 KAE  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K853708LARYNGASCOPES, FORCEPS, MICRO SUCTION TUBE & REFLEDowns Surgical , Ltd.1986-02-14
K85177519-790 TO 19-1042 DRESSING/SPONGE FORCEPSArtiberia1985-06-11
K85179441-180 TO 41-246 VARIOUS NASAL FORCEPSArtiberia1985-06-11
K85179541-250 TO 41-282 VARIOUS NASAL CUTTING FORCEPSArtiberia1985-06-11
K833608GOLD ALLIGATOR FORCEPSMicrotek Medical, Inc.1984-01-11
K833605CUPPED FORCEPSMicrotek Medical, Inc.1984-01-03
K833607MCGEE FORCEPSMicrotek Medical, Inc.1984-01-03
K822369MICRO & MINI-MICRO ALLIGATOR FORCEPSTreace Medical, Inc.1982-09-09
K822372OFFICE ECONO-FORCEPSTreace Medical, Inc.1982-09-09
K812895YARMO NASAL CARTILAGE SOFTENERAmerican V. Mueller1981-11-02
K772377HILDYARD POST NASAL FORCEPEdward Weck, Inc.1978-01-17
K772397COTTLE COLUMELLA FORCEPEdward Weck, Inc.1978-01-17
K772398COTTLE LOWER LATERAL FORCEPSEdward Weck, Inc.1978-01-17

Legacy Summary#

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FDA Review#

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