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FDA 510(k)

SONOMED 4000P ULTRASONIC PACHYMETER

K-Number: K924311 · 1992-12-08

ApplicantSonomed, Inc.
Decision Date1992-12-08
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SONOMED 4000P ULTRASONIC PACHYMETER is the device name listed in this FDA 510(k) record. The listed applicant is Sonomed, Inc.. It received FDA 510(k) clearance on 1992-12-08 under 510(k) number K924311. 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 SONOMED 4000P ULTRASONIC PACHYMETER?

SONOMED 4000P ULTRASONIC PACHYMETER is a medical device that received FDA 510(k) clearance on 1992-12-08. The listed applicant is Sonomed, Inc.. The 510(k) number is K924311.

When did SONOMED 4000P ULTRASONIC PACHYMETER receive FDA 510(k) clearance?

SONOMED 4000P ULTRASONIC PACHYMETER received FDA 510(k) clearance on 1992-12-08, under 510(k) number K924311.

Who is the listed applicant for SONOMED 4000P ULTRASONIC PACHYMETER?

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

What is the FDA product code for SONOMED 4000P ULTRASONIC PACHYMETER?

The FDA product code for SONOMED 4000P ULTRASONIC PACHYMETER 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 Sonomed, 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.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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