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FDA 510(k)

ACCESSORY FITMENT TO NEBULIZER SYSTEM, STERILE

K-Number: K901362 · 1990-06-06

Decision Date1990-06-06
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ACCESSORY FITMENT TO NEBULIZER SYSTEM, STERILE 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 1990-06-06 under 510(k) number K901362. 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 ACCESSORY FITMENT TO NEBULIZER SYSTEM, STERILE?

ACCESSORY FITMENT TO NEBULIZER SYSTEM, STERILE is a medical device that received FDA 510(k) clearance on 1990-06-06. The listed applicant is Automatic Liquid Packaging, Inc.. The 510(k) number is K901362.

When did ACCESSORY FITMENT TO NEBULIZER SYSTEM, STERILE receive FDA 510(k) clearance?

ACCESSORY FITMENT TO NEBULIZER SYSTEM, STERILE received FDA 510(k) clearance on 1990-06-06, under 510(k) number K901362.

Who is the listed applicant for ACCESSORY FITMENT TO NEBULIZER SYSTEM, STERILE?

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 ACCESSORY FITMENT TO NEBULIZER SYSTEM, STERILE?

The FDA product code for ACCESSORY FITMENT TO NEBULIZER SYSTEM, STERILE is CAF.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Automatic Liquid Packaging, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 21 devices →

Related Devices (Code: CAF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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