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510(k) K891023

Device
SIEMENS CEILING STAND 800F, 800 AND 810
Applicant
SIEMENS MEDICAL ELECTRONICS
510(k) number
K891023
Product code
LDQ
Decision
Substantially Equivalent (SESE)
Decision date
1989-07-25
Date received
1989-02-28
Regulation
510(k) Premarket Notification
Classification name
510(k) Premarket Notification // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Links U.S. Food & Drug Administration   Follow FDA En Español Search FDA   Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products   510(k) Premarket Notification Var MP = { Version: '1.0.22', Domains: {'es':'esp.fda.gov'}, SrcLang: 'en', UrlLang: 'mp_js_current_la
Medical specialty
General Hospital
Review panel
General Hospital
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
MURFITT, PHD
Address
16 Electronics Ave. Danvers MA US 01923 01923

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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