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FDA 510(k)

JETSTREAM G3 SYSTEM, MODEL PV31300, PV CONSOLE, MODEL PVCN100

K-Number: K101221 · 2010-06-02

Decision Date2010-06-02
Product CodeMCW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

JETSTREAM G3 SYSTEM, MODEL PV31300, PV CONSOLE, MODEL PVCN100 is the device name listed in this FDA 510(k) record. The listed applicant is Pathway Medical Technologies, Inc.. It received FDA 510(k) clearance on 2010-06-02 under 510(k) number K101221. The device is classified under product code MCW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JETSTREAM G3 SYSTEM, MODEL PV31300, PV CONSOLE, MODEL PVCN100?

JETSTREAM G3 SYSTEM, MODEL PV31300, PV CONSOLE, MODEL PVCN100 is a medical device that received FDA 510(k) clearance on 2010-06-02. The listed applicant is Pathway Medical Technologies, Inc.. The 510(k) number is K101221.

When did JETSTREAM G3 SYSTEM, MODEL PV31300, PV CONSOLE, MODEL PVCN100 receive FDA 510(k) clearance?

JETSTREAM G3 SYSTEM, MODEL PV31300, PV CONSOLE, MODEL PVCN100 received FDA 510(k) clearance on 2010-06-02, under 510(k) number K101221.

Who is the listed applicant for JETSTREAM G3 SYSTEM, MODEL PV31300, PV CONSOLE, MODEL PVCN100?

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

What is the FDA product code for JETSTREAM G3 SYSTEM, MODEL PV31300, PV CONSOLE, MODEL PVCN100?

The FDA product code for JETSTREAM G3 SYSTEM, MODEL PV31300, PV CONSOLE, MODEL PVCN100 is MCW.

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.

Other records listing Pathway Medical Technologies, 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.

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Related Devices (Code: MCW)

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.

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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