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FDA 510(k)

RESPIRIZER

K-Number: K810335 · 1981-03-20

ApplicantRespirizer Co., Div. Campillary Systems, Inc.
Decision Date1981-03-20
Product CodeKFZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RESPIRIZER is the device name listed in this FDA 510(k) record. The listed applicant is Respirizer Co., Div. Campillary Systems, Inc.. It received FDA 510(k) clearance on 1981-03-20 under 510(k) number K810335. The device is classified under product code KFZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RESPIRIZER?

RESPIRIZER is a medical device that received FDA 510(k) clearance on 1981-03-20. The listed applicant is Respirizer Co., Div. Campillary Systems, Inc.. The 510(k) number is K810335.

When did RESPIRIZER receive FDA 510(k) clearance?

RESPIRIZER received FDA 510(k) clearance on 1981-03-20, under 510(k) number K810335.

Who is the listed applicant for RESPIRIZER?

The FDA 510(k) record lists Respirizer Co., Div. Campillary Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RESPIRIZER?

The FDA product code for RESPIRIZER is KFZ.

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Related Devices (Code: KFZ)

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

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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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