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FDA 510(k)

CFI ULTRASOUND PROBE DRAPE

K-Number: K090773 · 2009-09-18

ApplicantContour Fabricators, Inc.
Decision Date2009-09-18
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CFI ULTRASOUND PROBE DRAPE is the device name listed in this FDA 510(k) record. The listed applicant is Contour Fabricators, Inc.. It received FDA 510(k) clearance on 2009-09-18 under 510(k) number K090773. 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 CFI ULTRASOUND PROBE DRAPE?

CFI ULTRASOUND PROBE DRAPE is a medical device that received FDA 510(k) clearance on 2009-09-18. The listed applicant is Contour Fabricators, Inc.. The 510(k) number is K090773.

When did CFI ULTRASOUND PROBE DRAPE receive FDA 510(k) clearance?

CFI ULTRASOUND PROBE DRAPE received FDA 510(k) clearance on 2009-09-18, under 510(k) number K090773.

Who is the listed applicant for CFI ULTRASOUND PROBE DRAPE?

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

What is the FDA product code for CFI ULTRASOUND PROBE DRAPE?

The FDA product code for CFI ULTRASOUND PROBE DRAPE is IYO.

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Other records listing Contour Fabricators, 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.

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Related Devices (Code: IYO)

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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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