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FDA 510(k)

HEWLETT PACKARD ULTRASOUND TRANSDUCER 21230A

K-Number: K854135 · 1985-12-23

ApplicantHewlett-Packard Co.
Decision Date1985-12-23
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

HEWLETT PACKARD ULTRASOUND TRANSDUCER 21230A is the device name listed in this FDA 510(k) record. The listed applicant is Hewlett-Packard Co.. It received FDA 510(k) clearance on 1985-12-23 under 510(k) number K854135. 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 HEWLETT PACKARD ULTRASOUND TRANSDUCER 21230A?

HEWLETT PACKARD ULTRASOUND TRANSDUCER 21230A is a medical device that received FDA 510(k) clearance on 1985-12-23. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K854135.

When did HEWLETT PACKARD ULTRASOUND TRANSDUCER 21230A receive FDA 510(k) clearance?

HEWLETT PACKARD ULTRASOUND TRANSDUCER 21230A received FDA 510(k) clearance on 1985-12-23, under 510(k) number K854135.

Who is the listed applicant for HEWLETT PACKARD ULTRASOUND TRANSDUCER 21230A?

The FDA 510(k) record lists Hewlett-Packard Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEWLETT PACKARD ULTRASOUND TRANSDUCER 21230A?

The FDA product code for HEWLETT PACKARD ULTRASOUND TRANSDUCER 21230A is IYO.

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Other records listing Hewlett-Packard Co. as applicant

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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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