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FDA 510(k)

UNIT DOSE 3% SODIUM CHLORIDE SOLUTION FOR INHALA.

K-Number: K884359 · 1988-12-20

ApplicantAutomatic Liquid Packaging, Inc.
Decision Date1988-12-20
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

UNIT DOSE 3% SODIUM CHLORIDE SOLUTION FOR INHALA. 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 1988-12-20 under 510(k) number K884359. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNIT DOSE 3% SODIUM CHLORIDE SOLUTION FOR INHALA.?

UNIT DOSE 3% SODIUM CHLORIDE SOLUTION FOR INHALA. is a medical device that received FDA 510(k) clearance on 1988-12-20. The listed applicant is Automatic Liquid Packaging, Inc.. The 510(k) number is K884359.

When did UNIT DOSE 3% SODIUM CHLORIDE SOLUTION FOR INHALA. receive FDA 510(k) clearance?

UNIT DOSE 3% SODIUM CHLORIDE SOLUTION FOR INHALA. received FDA 510(k) clearance on 1988-12-20, under 510(k) number K884359.

Who is the listed applicant for UNIT DOSE 3% SODIUM CHLORIDE SOLUTION FOR INHALA.?

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 UNIT DOSE 3% SODIUM CHLORIDE SOLUTION FOR INHALA.?

The FDA product code for UNIT DOSE 3% SODIUM CHLORIDE SOLUTION FOR INHALA. is CAF.

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Other records listing Automatic Liquid Packaging, Inc. as applicant

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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.

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