Decision Date1981-03-04
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
DAVOL ELECTRO MEDICAL SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1981-03-04 under 510(k) number K810273. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the DAVOL ELECTRO MEDICAL SYSTEMS?
DAVOL ELECTRO MEDICAL SYSTEMS is a medical device that received FDA 510(k) clearance on 1981-03-04. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K810273.
When did DAVOL ELECTRO MEDICAL SYSTEMS receive FDA 510(k) clearance?
DAVOL ELECTRO MEDICAL SYSTEMS received FDA 510(k) clearance on 1981-03-04, under 510(k) number K810273.
Who is the listed applicant for DAVOL ELECTRO MEDICAL SYSTEMS?
The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DAVOL ELECTRO MEDICAL SYSTEMS?
The FDA product code for DAVOL ELECTRO MEDICAL SYSTEMS is GEI.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.