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FDA 510(k)

POCKETSPACER

K-Number: K992038 · 1999-09-09

ApplicantFerraris Medical, Inc.
Decision Date1999-09-09
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

POCKETSPACER is the device name listed in this FDA 510(k) record. The listed applicant is Ferraris Medical, Inc.. It received FDA 510(k) clearance on 1999-09-09 under 510(k) number K992038. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POCKETSPACER?

POCKETSPACER is a medical device that received FDA 510(k) clearance on 1999-09-09. The listed applicant is Ferraris Medical, Inc.. The 510(k) number is K992038.

When did POCKETSPACER receive FDA 510(k) clearance?

POCKETSPACER received FDA 510(k) clearance on 1999-09-09, under 510(k) number K992038.

Who is the listed applicant for POCKETSPACER?

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

What is the FDA product code for POCKETSPACER?

The FDA product code for POCKETSPACER is CAF.

Related Clinical Trials

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Other records listing Ferraris Medical, 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.

K993199POCKET CHAMBER VALVED AEROSOL HOLDING CHAMBERK924343WRIGHT POCKET PEAK FLOW METER

Related Devices (Code: CAF)

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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