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FDA 510(k)

LIFESYNC ADAPTER, MODEL LS-302

K-Number: K071751 · 2007-08-27

ApplicantLifesync Corporation
Decision Date2007-08-27
Product CodeDSA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LIFESYNC ADAPTER, MODEL LS-302 is the device name listed in this FDA 510(k) record. The listed applicant is Lifesync Corporation. It received FDA 510(k) clearance on 2007-08-27 under 510(k) number K071751. The device is classified under product code DSA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIFESYNC ADAPTER, MODEL LS-302?

LIFESYNC ADAPTER, MODEL LS-302 is a medical device that received FDA 510(k) clearance on 2007-08-27. The listed applicant is Lifesync Corporation. The 510(k) number is K071751.

When did LIFESYNC ADAPTER, MODEL LS-302 receive FDA 510(k) clearance?

LIFESYNC ADAPTER, MODEL LS-302 received FDA 510(k) clearance on 2007-08-27, under 510(k) number K071751.

Who is the listed applicant for LIFESYNC ADAPTER, MODEL LS-302?

The FDA 510(k) record lists Lifesync Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIFESYNC ADAPTER, MODEL LS-302?

The FDA product code for LIFESYNC ADAPTER, MODEL LS-302 is DSA.

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Official Source

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