Decision Date1998-09-10
Product CodeMED
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
CETYLCIDE-G is the device name listed in this FDA 510(k) record. The listed applicant is Kellerandheckman. It received FDA 510(k) clearance on 1998-09-10 under 510(k) number K974188. The device is classified under product code MED. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the CETYLCIDE-G?
CETYLCIDE-G is a medical device that received FDA 510(k) clearance on 1998-09-10. The listed applicant is Kellerandheckman. The 510(k) number is K974188.
When did CETYLCIDE-G receive FDA 510(k) clearance?
CETYLCIDE-G received FDA 510(k) clearance on 1998-09-10, under 510(k) number K974188.
Who is the listed applicant for CETYLCIDE-G?
The FDA 510(k) record lists Kellerandheckman as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CETYLCIDE-G?
The FDA product code for CETYLCIDE-G is MED.
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Official Source
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