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FDA 510(k)

AGILANCE-GOLDEN SPOONS

K-Number: K936178 · 1995-01-18

ApplicantOismuller & Partner Keg
Decision Date1995-01-18
Product CodeISA
Advisory CommitteePM
DecisionSubstantially Equivalent for Some Indications

Device Summary

AGILANCE-GOLDEN SPOONS is the device name listed in this FDA 510(k) record. The listed applicant is Oismuller & Partner Keg. It received FDA 510(k) clearance on 1995-01-18 under 510(k) number K936178. The device is classified under product code ISA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the AGILANCE-GOLDEN SPOONS?

AGILANCE-GOLDEN SPOONS is a medical device that received FDA 510(k) clearance on 1995-01-18. The listed applicant is Oismuller & Partner Keg. The 510(k) number is K936178.

When did AGILANCE-GOLDEN SPOONS receive FDA 510(k) clearance?

AGILANCE-GOLDEN SPOONS received FDA 510(k) clearance on 1995-01-18, under 510(k) number K936178.

Who is the listed applicant for AGILANCE-GOLDEN SPOONS?

The FDA 510(k) record lists Oismuller & Partner Keg as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AGILANCE-GOLDEN SPOONS?

The FDA product code for AGILANCE-GOLDEN SPOONS is ISA.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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