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FDA 510(k)

PERCEPTION INC. GPS-XYZ DIAGNOSTIC ULTRASOUND SYSTEM

K-Number: K972192 · 1997-12-17

ApplicantPerception, Inc.
Decision Date1997-12-17
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PERCEPTION INC. GPS-XYZ DIAGNOSTIC ULTRASOUND SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Perception, Inc.. It received FDA 510(k) clearance on 1997-12-17 under 510(k) number K972192. 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 PERCEPTION INC. GPS-XYZ DIAGNOSTIC ULTRASOUND SYSTEM?

PERCEPTION INC. GPS-XYZ DIAGNOSTIC ULTRASOUND SYSTEM is a medical device that received FDA 510(k) clearance on 1997-12-17. The listed applicant is Perception, Inc.. The 510(k) number is K972192.

When did PERCEPTION INC. GPS-XYZ DIAGNOSTIC ULTRASOUND SYSTEM receive FDA 510(k) clearance?

PERCEPTION INC. GPS-XYZ DIAGNOSTIC ULTRASOUND SYSTEM received FDA 510(k) clearance on 1997-12-17, under 510(k) number K972192.

Who is the listed applicant for PERCEPTION INC. GPS-XYZ DIAGNOSTIC ULTRASOUND SYSTEM?

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

What is the FDA product code for PERCEPTION INC. GPS-XYZ DIAGNOSTIC ULTRASOUND SYSTEM?

The FDA product code for PERCEPTION INC. GPS-XYZ DIAGNOSTIC ULTRASOUND SYSTEM is IYO.

Related Clinical Trials

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Other records listing Perception, 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.

K981834PERCEPTION INC, GPS-6TBMD DIAGNOSTIC ULTRASOUND SYSTEMK974880PERCEPTION GPS-RST DIAGNOSTIC ULTRASOUND SYSTEMK972973PERCEPTION INC. GPS-TUV DIAGNOSTIC ULTRASOUND SYSTEM

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.

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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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