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FDA 510(k)

CANNULAE, PLASTIC DISPOSABLE NASAL

K-Number: K760218 · 1976-08-03

Decision Date1976-08-03
Product CodeCAT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CANNULAE, PLASTIC DISPOSABLE NASAL is the device name listed in this FDA 510(k) record. The listed applicant is Manner Medical Products. It received FDA 510(k) clearance on 1976-08-03 under 510(k) number K760218. 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 CANNULAE, PLASTIC DISPOSABLE NASAL?

CANNULAE, PLASTIC DISPOSABLE NASAL is a medical device that received FDA 510(k) clearance on 1976-08-03. The listed applicant is Manner Medical Products. The 510(k) number is K760218.

When did CANNULAE, PLASTIC DISPOSABLE NASAL receive FDA 510(k) clearance?

CANNULAE, PLASTIC DISPOSABLE NASAL received FDA 510(k) clearance on 1976-08-03, under 510(k) number K760218.

Who is the listed applicant for CANNULAE, PLASTIC DISPOSABLE NASAL?

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

What is the FDA product code for CANNULAE, PLASTIC DISPOSABLE NASAL?

The FDA product code for CANNULAE, PLASTIC DISPOSABLE NASAL 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 Manner Medical Products 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: 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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