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FDA 510(k)

VOYAGER/X

K-Number: K884754 · 1989-01-04

ApplicantSmith-Perry Corp.
Decision Date1989-01-04
Product CodeNFB
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VOYAGER/X is the device name listed in this FDA 510(k) record. The listed applicant is Smith-Perry Corp.. It received FDA 510(k) clearance on 1989-01-04 under 510(k) number K884754. The device is classified under product code NFB. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VOYAGER/X?

VOYAGER/X is a medical device that received FDA 510(k) clearance on 1989-01-04. The listed applicant is Smith-Perry Corp.. The 510(k) number is K884754.

When did VOYAGER/X receive FDA 510(k) clearance?

VOYAGER/X received FDA 510(k) clearance on 1989-01-04, under 510(k) number K884754.

Who is the listed applicant for VOYAGER/X?

The FDA 510(k) record lists Smith-Perry Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VOYAGER/X?

The FDA product code for VOYAGER/X is NFB.

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.

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Other records listing Smith-Perry Corp. 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.

K895082VOYAGER PX

Related Devices (Code: NFB)

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.

K250322Respond OC Conserving Regulator (130-0800)Responsive RespiratoryK220591ProximaDynasthetics, LLCK221014Effortless Oxygen Conserver System Models Effortless Pro and Effortless MobileEffortless Oxygen, LLCK200401ApogeeIncoba Ltd D/B/A DynarisK151506Demand Nasal Oxygen Cannula, Modified Demand Nasal Oxygen CannulaSalter LabsK131023THERAFLOW SINGLE LUMEN AND THERAFLOW DUAL LUMENMedical Products, LLC

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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