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510(k) K771864

Device
WALL TRANSFORMERS 74710 & 74910
Applicant
WELCH ALLYN, INC.
510(k) number
K771864
Product code
GCW  
Decision
Substantially Equivalent (SESE)
Decision date
1977-11-22
Date received
1977-10-03
Regulation
876.1500
Classification name
Transformer, Endoscope
Medical specialty
Gastroenterology/Urology
Review panel
Gastroenterology/Urology
Device class
2
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

Legacy Summary#

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FDA Review#

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