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FDA 510(k)

MEDICOMP CPAP NASAL CANNULA

K-Number: K861280 · 1986-05-09

Decision Date1986-05-09
Product CodeBZD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MEDICOMP CPAP NASAL CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Medicomp, Inc.. It received FDA 510(k) clearance on 1986-05-09 under 510(k) number K861280. The device is classified under product code BZD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDICOMP CPAP NASAL CANNULA?

MEDICOMP CPAP NASAL CANNULA is a medical device that received FDA 510(k) clearance on 1986-05-09. The listed applicant is Medicomp, Inc.. The 510(k) number is K861280.

When did MEDICOMP CPAP NASAL CANNULA receive FDA 510(k) clearance?

MEDICOMP CPAP NASAL CANNULA received FDA 510(k) clearance on 1986-05-09, under 510(k) number K861280.

Who is the listed applicant for MEDICOMP CPAP NASAL CANNULA?

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

What is the FDA product code for MEDICOMP CPAP NASAL CANNULA?

The FDA product code for MEDICOMP CPAP NASAL CANNULA is BZD.

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 Medicomp, 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 23 devices →

Related Devices (Code: BZD)

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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