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FDA 510(k)

AMERIMED AS110

K-Number: K953069 · 1995-08-31

ApplicantAmerimed Systems L.C.
Decision Date1995-08-31
Product CodeFNM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AMERIMED AS110 is the device name listed in this FDA 510(k) record. The listed applicant is Amerimed Systems L.C.. It received FDA 510(k) clearance on 1995-08-31 under 510(k) number K953069. The device is classified under product code FNM. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMERIMED AS110?

AMERIMED AS110 is a medical device that received FDA 510(k) clearance on 1995-08-31. The listed applicant is Amerimed Systems L.C.. The 510(k) number is K953069.

When did AMERIMED AS110 receive FDA 510(k) clearance?

AMERIMED AS110 received FDA 510(k) clearance on 1995-08-31, under 510(k) number K953069.

Who is the listed applicant for AMERIMED AS110?

The FDA 510(k) record lists Amerimed Systems L.C. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AMERIMED AS110?

The FDA product code for AMERIMED AS110 is FNM.

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Related Devices (Code: FNM)

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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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