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FDA 510(k)

PRIME CARE NEONATAL/PEDIATRIC TRACHEOSTOMY TUBE

K-Number: K901920 · 1990-08-17

Decision Date1990-08-17
Product CodeBTO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PRIME CARE NEONATAL/PEDIATRIC TRACHEOSTOMY TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Primecare, Inc.. It received FDA 510(k) clearance on 1990-08-17 under 510(k) number K901920. The device is classified under product code BTO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRIME CARE NEONATAL/PEDIATRIC TRACHEOSTOMY TUBE?

PRIME CARE NEONATAL/PEDIATRIC TRACHEOSTOMY TUBE is a medical device that received FDA 510(k) clearance on 1990-08-17. The listed applicant is Primecare, Inc.. The 510(k) number is K901920.

When did PRIME CARE NEONATAL/PEDIATRIC TRACHEOSTOMY TUBE receive FDA 510(k) clearance?

PRIME CARE NEONATAL/PEDIATRIC TRACHEOSTOMY TUBE received FDA 510(k) clearance on 1990-08-17, under 510(k) number K901920.

Who is the listed applicant for PRIME CARE NEONATAL/PEDIATRIC TRACHEOSTOMY TUBE?

The FDA 510(k) record lists Primecare, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PRIME CARE NEONATAL/PEDIATRIC TRACHEOSTOMY TUBE?

The FDA product code for PRIME CARE NEONATAL/PEDIATRIC TRACHEOSTOMY TUBE is BTO.

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.

Related Devices (Code: BTO)

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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