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FDA 510(k)

SALTER LABS NEONATAL NASAL OXYGEN CANNULA

K-Number: K911740 · 1991-07-24

ApplicantSalter Labs
Decision Date1991-07-24
Product CodeCAT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SALTER LABS NEONATAL NASAL OXYGEN CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Salter Labs. It received FDA 510(k) clearance on 1991-07-24 under 510(k) number K911740. The device is classified under product code CAT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SALTER LABS NEONATAL NASAL OXYGEN CANNULA?

SALTER LABS NEONATAL NASAL OXYGEN CANNULA is a medical device that received FDA 510(k) clearance on 1991-07-24. The listed applicant is Salter Labs. The 510(k) number is K911740.

When did SALTER LABS NEONATAL NASAL OXYGEN CANNULA receive FDA 510(k) clearance?

SALTER LABS NEONATAL NASAL OXYGEN CANNULA received FDA 510(k) clearance on 1991-07-24, under 510(k) number K911740.

Who is the listed applicant for SALTER LABS NEONATAL NASAL OXYGEN CANNULA?

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

What is the FDA product code for SALTER LABS NEONATAL NASAL OXYGEN CANNULA?

The FDA product code for SALTER LABS NEONATAL NASAL OXYGEN CANNULA is CAT.

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 Salter Labs 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 47 devices →

Related Devices (Code: CAT)

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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