TRACHEOSTOMY & NASAL SUCTIONING KIT, 3C-TNS-1
K-Number: K871692 · 1987-06-01
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Device Summary
Frequently Asked Questions
What is the TRACHEOSTOMY & NASAL SUCTIONING KIT, 3C-TNS-1?
TRACHEOSTOMY & NASAL SUCTIONING KIT, 3C-TNS-1 is a medical device that received FDA 510(k) clearance on 1987-06-01. The listed applicant is Automatic Liquid Packaging, Inc.. The 510(k) number is K871692.
When did TRACHEOSTOMY & NASAL SUCTIONING KIT, 3C-TNS-1 receive FDA 510(k) clearance?
TRACHEOSTOMY & NASAL SUCTIONING KIT, 3C-TNS-1 received FDA 510(k) clearance on 1987-06-01, under 510(k) number K871692.
Who is the listed applicant for TRACHEOSTOMY & NASAL SUCTIONING KIT, 3C-TNS-1?
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 TRACHEOSTOMY & NASAL SUCTIONING KIT, 3C-TNS-1?
The FDA product code for TRACHEOSTOMY & NASAL SUCTIONING KIT, 3C-TNS-1 is LRQ.
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: LRQ)
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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