ACCESSORY FITMENT TO NEBULIZER SYSTEM, STERILE
K-Number: K901362 · 1990-06-06
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Device Summary
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.
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
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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