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FDA 510(k)

RHYTHM TOUCH Q 2-WAY

K-Number: K032178 · 2003-10-15

ApplicantShockim Enterprises, Ltd.
Decision Date2003-10-15
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

RHYTHM TOUCH Q 2-WAY is the device name listed in this FDA 510(k) record. The listed applicant is Shockim Enterprises, Ltd.. It received FDA 510(k) clearance on 2003-10-15 under 510(k) number K032178. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RHYTHM TOUCH Q 2-WAY?

RHYTHM TOUCH Q 2-WAY is a medical device that received FDA 510(k) clearance on 2003-10-15. The listed applicant is Shockim Enterprises, Ltd.. The 510(k) number is K032178.

When did RHYTHM TOUCH Q 2-WAY receive FDA 510(k) clearance?

RHYTHM TOUCH Q 2-WAY received FDA 510(k) clearance on 2003-10-15, under 510(k) number K032178.

Who is the listed applicant for RHYTHM TOUCH Q 2-WAY?

The FDA 510(k) record lists Shockim Enterprises, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RHYTHM TOUCH Q 2-WAY?

The FDA product code for RHYTHM TOUCH Q 2-WAY is IPF.

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Other records listing Shockim Enterprises, Ltd. 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.

K063743RHYTHM TOUCH Q 2-WAY

Related Devices (Code: IPF)

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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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