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FDA 510(k)

STERISIL ANTIMICROBIAL TUBING AND BOTTLE

K-Number: K031681 · 2003-10-30

ApplicantSterisil
Decision Date2003-10-30
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

STERISIL ANTIMICROBIAL TUBING AND BOTTLE is the device name listed in this FDA 510(k) record. The listed applicant is Sterisil. It received FDA 510(k) clearance on 2003-10-30 under 510(k) number K031681. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERISIL ANTIMICROBIAL TUBING AND BOTTLE?

STERISIL ANTIMICROBIAL TUBING AND BOTTLE is a medical device that received FDA 510(k) clearance on 2003-10-30. The listed applicant is Sterisil. The 510(k) number is K031681.

When did STERISIL ANTIMICROBIAL TUBING AND BOTTLE receive FDA 510(k) clearance?

STERISIL ANTIMICROBIAL TUBING AND BOTTLE received FDA 510(k) clearance on 2003-10-30, under 510(k) number K031681.

Who is the listed applicant for STERISIL ANTIMICROBIAL TUBING AND BOTTLE?

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

What is the FDA product code for STERISIL ANTIMICROBIAL TUBING AND BOTTLE?

The FDA product code for STERISIL ANTIMICROBIAL TUBING AND BOTTLE is EIA.

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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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