FDA 510(k)

AMPERCIDE DISINFECTANT ACCESSORY TO -

K-Number: K830881 · 1983-06-02

ApplicantAmerican Medical Products, Inc.

Decision Date1983-06-02

Product CodeFKX

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

AMPERCIDE DISINFECTANT ACCESSORY TO - is the device name listed in this FDA 510(k) record. The listed applicant is American Medical Products, Inc.. It received FDA 510(k) clearance on 1983-06-02 under 510(k) number K830881. The device is classified under product code FKX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMPERCIDE DISINFECTANT ACCESSORY TO -?

AMPERCIDE DISINFECTANT ACCESSORY TO - is a medical device that received FDA 510(k) clearance on 1983-06-02. The listed applicant is American Medical Products, Inc.. The 510(k) number is K830881.

When did AMPERCIDE DISINFECTANT ACCESSORY TO - receive FDA 510(k) clearance?

AMPERCIDE DISINFECTANT ACCESSORY TO - received FDA 510(k) clearance on 1983-06-02, under 510(k) number K830881.

Who is the listed applicant for AMPERCIDE DISINFECTANT ACCESSORY TO -?

The FDA 510(k) record lists American Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AMPERCIDE DISINFECTANT ACCESSORY TO -?

The FDA product code for AMPERCIDE DISINFECTANT ACCESSORY TO - is FKX.

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Official Source

View on FDA Database →

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