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FDA 510(k)

POCKET ULTRASONIC PACHYMETER

K-Number: K993674 · 2000-07-13

ApplicantQuantel Medical
Decision Date2000-07-13
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

POCKET ULTRASONIC PACHYMETER is the device name listed in this FDA 510(k) record. The listed applicant is Quantel Medical. It received FDA 510(k) clearance on 2000-07-13 under 510(k) number K993674. 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 POCKET ULTRASONIC PACHYMETER?

POCKET ULTRASONIC PACHYMETER is a medical device that received FDA 510(k) clearance on 2000-07-13. The listed applicant is Quantel Medical. The 510(k) number is K993674.

When did POCKET ULTRASONIC PACHYMETER receive FDA 510(k) clearance?

POCKET ULTRASONIC PACHYMETER received FDA 510(k) clearance on 2000-07-13, under 510(k) number K993674.

Who is the listed applicant for POCKET ULTRASONIC PACHYMETER?

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

What is the FDA product code for POCKET ULTRASONIC PACHYMETER?

The FDA product code for POCKET ULTRASONIC PACHYMETER is IYO.

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Other records listing Quantel Medical 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)

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.

K260313MD-6000S Bladder ScannerMEDA Co., Ltd.K253452Accuro 3SRivanna Medical, Inc.K260190ARTHURROPCA ApSK252237EdgeFlow UW20Edgecare, Inc.K254021Accuro XVRivanna Medical, Inc.K253898QT Scanner 2000 Model AQT Imaging Holdings, Inc.

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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