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FDA 510(k)

PHILIPS HEARTSTART 12 LEAD TRANSFER STATION, MODEL 989803142521

K-Number: K071391 · 2007-09-07

Decision Date2007-09-07
Product CodeMSX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PHILIPS HEARTSTART 12 LEAD TRANSFER STATION, MODEL 989803142521 is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems, Inc.. It received FDA 510(k) clearance on 2007-09-07 under 510(k) number K071391. The device is classified under product code MSX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHILIPS HEARTSTART 12 LEAD TRANSFER STATION, MODEL 989803142521?

PHILIPS HEARTSTART 12 LEAD TRANSFER STATION, MODEL 989803142521 is a medical device that received FDA 510(k) clearance on 2007-09-07. The listed applicant is Philips Medical Systems, Inc.. The 510(k) number is K071391.

When did PHILIPS HEARTSTART 12 LEAD TRANSFER STATION, MODEL 989803142521 receive FDA 510(k) clearance?

PHILIPS HEARTSTART 12 LEAD TRANSFER STATION, MODEL 989803142521 received FDA 510(k) clearance on 2007-09-07, under 510(k) number K071391.

Who is the listed applicant for PHILIPS HEARTSTART 12 LEAD TRANSFER STATION, MODEL 989803142521?

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

What is the FDA product code for PHILIPS HEARTSTART 12 LEAD TRANSFER STATION, MODEL 989803142521?

The FDA product code for PHILIPS HEARTSTART 12 LEAD TRANSFER STATION, MODEL 989803142521 is MSX.

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 Philips Medical Systems, 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.

View all 111 devices →

Related Devices (Code: MSX)

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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