Decision Date1977-04-28
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
ELECTROSURGICAL PATIENT GROUNDING PAD 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 1977-04-28 under 510(k) number K770646. 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 ELECTROSURGICAL PATIENT GROUNDING PAD?
ELECTROSURGICAL PATIENT GROUNDING PAD is a medical device that received FDA 510(k) clearance on 1977-04-28. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K770646.
When did ELECTROSURGICAL PATIENT GROUNDING PAD receive FDA 510(k) clearance?
ELECTROSURGICAL PATIENT GROUNDING PAD received FDA 510(k) clearance on 1977-04-28, under 510(k) number K770646.
Who is the listed applicant for ELECTROSURGICAL PATIENT GROUNDING PAD?
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 ELECTROSURGICAL PATIENT GROUNDING PAD?
The FDA product code for ELECTROSURGICAL PATIENT GROUNDING PAD is GEI.
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Official Source
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