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FDA 510(k)

NEONATAL CANNULA CAP

K-Number: K864883 · 1987-01-28

ApplicantBehan & Taylor Ent.
Decision Date1987-01-28
Product CodeBZD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NEONATAL CANNULA CAP is the device name listed in this FDA 510(k) record. The listed applicant is Behan & Taylor Ent.. It received FDA 510(k) clearance on 1987-01-28 under 510(k) number K864883. 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 NEONATAL CANNULA CAP?

NEONATAL CANNULA CAP is a medical device that received FDA 510(k) clearance on 1987-01-28. The listed applicant is Behan & Taylor Ent.. The 510(k) number is K864883.

When did NEONATAL CANNULA CAP receive FDA 510(k) clearance?

NEONATAL CANNULA CAP received FDA 510(k) clearance on 1987-01-28, under 510(k) number K864883.

Who is the listed applicant for NEONATAL CANNULA CAP?

The FDA 510(k) record lists Behan & Taylor Ent. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEONATAL CANNULA CAP?

The FDA product code for NEONATAL CANNULA CAP is BZD.

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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.

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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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