FDA 510(k)

SITE-RITE 6 ULTRASOUND SYSTEM, MODEL SITE-RITE 6

K-Number: K071204 · 2007-05-18

Decision Date2007-05-18

Product CodeIYO

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

SITE-RITE 6 ULTRASOUND SYSTEM, MODEL SITE-RITE 6 is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 2007-05-18 under 510(k) number K071204. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SITE-RITE 6 ULTRASOUND SYSTEM, MODEL SITE-RITE 6?

SITE-RITE 6 ULTRASOUND SYSTEM, MODEL SITE-RITE 6 is a medical device that received FDA 510(k) clearance on 2007-05-18. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K071204.

When did SITE-RITE 6 ULTRASOUND SYSTEM, MODEL SITE-RITE 6 receive FDA 510(k) clearance?

SITE-RITE 6 ULTRASOUND SYSTEM, MODEL SITE-RITE 6 received FDA 510(k) clearance on 2007-05-18, under 510(k) number K071204.

Who is the listed applicant for SITE-RITE 6 ULTRASOUND SYSTEM, MODEL SITE-RITE 6?

The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SITE-RITE 6 ULTRASOUND SYSTEM, MODEL SITE-RITE 6?

The FDA product code for SITE-RITE 6 ULTRASOUND SYSTEM, MODEL SITE-RITE 6 is IYO.

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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.