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FDA 510(k)

SYMMETRY IQ, MODEL 2000 SERIES, 3000 SERIES

K-Number: K070975 · 2007-06-21

ApplicantHu-Friedy Mfg. Co., Inc.
Decision Date2007-06-21
Product CodeELC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SYMMETRY IQ, MODEL 2000 SERIES, 3000 SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Hu-Friedy Mfg. Co., Inc.. It received FDA 510(k) clearance on 2007-06-21 under 510(k) number K070975. The device is classified under product code ELC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYMMETRY IQ, MODEL 2000 SERIES, 3000 SERIES?

SYMMETRY IQ, MODEL 2000 SERIES, 3000 SERIES is a medical device that received FDA 510(k) clearance on 2007-06-21. The listed applicant is Hu-Friedy Mfg. Co., Inc.. The 510(k) number is K070975.

When did SYMMETRY IQ, MODEL 2000 SERIES, 3000 SERIES receive FDA 510(k) clearance?

SYMMETRY IQ, MODEL 2000 SERIES, 3000 SERIES received FDA 510(k) clearance on 2007-06-21, under 510(k) number K070975.

Who is the listed applicant for SYMMETRY IQ, MODEL 2000 SERIES, 3000 SERIES?

The FDA 510(k) record lists Hu-Friedy Mfg. Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SYMMETRY IQ, MODEL 2000 SERIES, 3000 SERIES?

The FDA product code for SYMMETRY IQ, MODEL 2000 SERIES, 3000 SERIES is ELC.

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Official Source

View on FDA Database →

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

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