FDA 510(k)

STERILE WATER OR O.9% SODIUM CHLORIDE, MODEL AL4100 & AL4109

K-Number: K000964 · 2000-04-25

ApplicantAutomatic Liquid Packaging, Inc.

Decision Date2000-04-25

Product CodeJOH

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

STERILE WATER OR O.9% SODIUM CHLORIDE, MODEL AL4100 & AL4109 is the device name listed in this FDA 510(k) record. The listed applicant is Automatic Liquid Packaging, Inc.. It received FDA 510(k) clearance on 2000-04-25 under 510(k) number K000964. The device is classified under product code JOH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILE WATER OR O.9% SODIUM CHLORIDE, MODEL AL4100 & AL4109?

STERILE WATER OR O.9% SODIUM CHLORIDE, MODEL AL4100 & AL4109 is a medical device that received FDA 510(k) clearance on 2000-04-25. The listed applicant is Automatic Liquid Packaging, Inc.. The 510(k) number is K000964.

When did STERILE WATER OR O.9% SODIUM CHLORIDE, MODEL AL4100 & AL4109 receive FDA 510(k) clearance?

STERILE WATER OR O.9% SODIUM CHLORIDE, MODEL AL4100 & AL4109 received FDA 510(k) clearance on 2000-04-25, under 510(k) number K000964.

Who is the listed applicant for STERILE WATER OR O.9% SODIUM CHLORIDE, MODEL AL4100 & AL4109?

The FDA 510(k) record lists Automatic Liquid Packaging, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STERILE WATER OR O.9% SODIUM CHLORIDE, MODEL AL4100 & AL4109?

The FDA product code for STERILE WATER OR O.9% SODIUM CHLORIDE, MODEL AL4100 & AL4109 is JOH.

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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.