Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

TRACHEOSTOMY & NASAL SUCTIONING KIT, 3C-TNS-1

K-Number: K871692 · 1987-06-01

Decision Date1987-06-01
Product CodeLRQ
DecisionSubstantially Equivalent

Device Summary

TRACHEOSTOMY & NASAL SUCTIONING KIT, 3C-TNS-1 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 1987-06-01 under 510(k) number K871692. The device is classified under product code LRQ. FDA Decision: Substantially Equivalent.

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.

View all 21 devices →

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.

↑