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FDA 510(k)

CETYLCIDE-G

K-Number: K974188 · 1998-09-10

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.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: MED)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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