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FDA 510(k)

DIAGNOSTIC ULTRASOUND UFS 1005

K-Number: K902408 · 1990-08-10

ApplicantDiagnostic Ultrasound Corp.
Decision Date1990-08-10
Product CodeEXY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DIAGNOSTIC ULTRASOUND UFS 1005 is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostic Ultrasound Corp.. It received FDA 510(k) clearance on 1990-08-10 under 510(k) number K902408. The device is classified under product code EXY. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIAGNOSTIC ULTRASOUND UFS 1005?

DIAGNOSTIC ULTRASOUND UFS 1005 is a medical device that received FDA 510(k) clearance on 1990-08-10. The listed applicant is Diagnostic Ultrasound Corp.. The 510(k) number is K902408.

When did DIAGNOSTIC ULTRASOUND UFS 1005 receive FDA 510(k) clearance?

DIAGNOSTIC ULTRASOUND UFS 1005 received FDA 510(k) clearance on 1990-08-10, under 510(k) number K902408.

Who is the listed applicant for DIAGNOSTIC ULTRASOUND UFS 1005?

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

What is the FDA product code for DIAGNOSTIC ULTRASOUND UFS 1005?

The FDA product code for DIAGNOSTIC ULTRASOUND UFS 1005 is EXY.

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Other records listing Diagnostic Ultrasound Corp. 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.

K030763DIAGNOSTIC ULTRASOUND BLADDERMASS BVM 6500 ULTRASOUND SYSTEMK022153BLADDERSCAN BVI 6100K982568BLADDERMANAGER PCI 5000 MODEL 1002K963585BLADDER MANAGER PCI 5000, BLADDERSCAN BVI 5000K955840BLADDERMANAGER PCI 5000 / BLADDERSCAN BVI 5000K955942BLADDERSCAN BVI 5000

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Related Devices (Code: EXY)

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.

K022721UROPOWERW.O.M. World of Medicine AGK971913GR100F URINE FLOWMETERAlbyn Medical , Ltd.K953999DANTEC DA CAPODantec Medical, Inc.K951442FLOLABSynectics Medical, Inc.K944972URO-GRAM CYSTOMRTROGRAM WITH UROFLOWMETRYMyo/Kinetic Systems, Inc.K9454954-CHANNEL URODYNAMIC MONITOR WITH URO-FLO OPTIONFiberoptic Sensor Technlogies, 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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