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FDA 510(k)

ULTRASOUND SCANNER, TYPE 2102

K-Number: K011417 · 2001-06-08

Decision Date2001-06-08
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ULTRASOUND SCANNER, TYPE 2102 is the device name listed in this FDA 510(k) record. The listed applicant is B-K Medical A/S. It received FDA 510(k) clearance on 2001-06-08 under 510(k) number K011417. 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 ULTRASOUND SCANNER, TYPE 2102?

ULTRASOUND SCANNER, TYPE 2102 is a medical device that received FDA 510(k) clearance on 2001-06-08. The listed applicant is B-K Medical A/S. The 510(k) number is K011417.

When did ULTRASOUND SCANNER, TYPE 2102 receive FDA 510(k) clearance?

ULTRASOUND SCANNER, TYPE 2102 received FDA 510(k) clearance on 2001-06-08, under 510(k) number K011417.

Who is the listed applicant for ULTRASOUND SCANNER, TYPE 2102?

The FDA 510(k) record lists B-K Medical A/S as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ULTRASOUND SCANNER, TYPE 2102?

The FDA product code for ULTRASOUND SCANNER, TYPE 2102 is IYO.

Related Clinical Trials

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.

Other records listing B-K Medical A/S 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.

View all 7 devices →

Related Devices (Code: IYO)

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.

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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