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FDA 510(k)

RESPIFLO/S

K-Number: K962874 · 1997-02-25

ApplicantCurtin & Associates International , Inc.
Decision Date1997-02-25
Product CodeCAF
Advisory CommitteeAN
DecisionUnknown

Device Summary

RESPIFLO/S is the device name listed in this FDA 510(k) record. The listed applicant is Curtin & Associates International , Inc.. It received FDA 510(k) clearance on 1997-02-25 under 510(k) number K962874. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the RESPIFLO/S?

RESPIFLO/S is a medical device that received FDA 510(k) clearance on 1997-02-25. The listed applicant is Curtin & Associates International , Inc.. The 510(k) number is K962874.

When did RESPIFLO/S receive FDA 510(k) clearance?

RESPIFLO/S received FDA 510(k) clearance on 1997-02-25, under 510(k) number K962874.

Who is the listed applicant for RESPIFLO/S?

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

What is the FDA product code for RESPIFLO/S?

The FDA product code for RESPIFLO/S is CAF.

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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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