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FDA 510(k)

PREFILLED RESPIRATORY THERAPY VIAL

K-Number: K830943 · 1983-04-28

ApplicantAutomatic Liquid Packaging, Inc.
Decision Date1983-04-28
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PREFILLED RESPIRATORY THERAPY VIAL 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 1983-04-28 under 510(k) number K830943. 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 PREFILLED RESPIRATORY THERAPY VIAL?

PREFILLED RESPIRATORY THERAPY VIAL is a medical device that received FDA 510(k) clearance on 1983-04-28. The listed applicant is Automatic Liquid Packaging, Inc.. The 510(k) number is K830943.

When did PREFILLED RESPIRATORY THERAPY VIAL receive FDA 510(k) clearance?

PREFILLED RESPIRATORY THERAPY VIAL received FDA 510(k) clearance on 1983-04-28, under 510(k) number K830943.

Who is the listed applicant for PREFILLED RESPIRATORY THERAPY VIAL?

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 PREFILLED RESPIRATORY THERAPY VIAL?

The FDA product code for PREFILLED RESPIRATORY THERAPY VIAL is CAF.

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Related Devices (Code: CAF)

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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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