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FDA 510(k)

INTERSON MULTIPLANE RECTAL PROBE FOR ALOKA ULTRA.

K-Number: K900555 · 1990-05-02

ApplicantInterson Corp.
Decision Date1990-05-02
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

INTERSON MULTIPLANE RECTAL PROBE FOR ALOKA ULTRA. is the device name listed in this FDA 510(k) record. The listed applicant is Interson Corp.. It received FDA 510(k) clearance on 1990-05-02 under 510(k) number K900555. The device is classified under product code ITX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTERSON MULTIPLANE RECTAL PROBE FOR ALOKA ULTRA.?

INTERSON MULTIPLANE RECTAL PROBE FOR ALOKA ULTRA. is a medical device that received FDA 510(k) clearance on 1990-05-02. The listed applicant is Interson Corp.. The 510(k) number is K900555.

When did INTERSON MULTIPLANE RECTAL PROBE FOR ALOKA ULTRA. receive FDA 510(k) clearance?

INTERSON MULTIPLANE RECTAL PROBE FOR ALOKA ULTRA. received FDA 510(k) clearance on 1990-05-02, under 510(k) number K900555.

Who is the listed applicant for INTERSON MULTIPLANE RECTAL PROBE FOR ALOKA ULTRA.?

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

What is the FDA product code for INTERSON MULTIPLANE RECTAL PROBE FOR ALOKA ULTRA.?

The FDA product code for INTERSON MULTIPLANE RECTAL PROBE FOR ALOKA ULTRA. is ITX.

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Other records listing Interson 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.

K911116INTERSON ENDOCAVITY PROBE/KONTRON ULTRASOUND SYSTK911115INTERSON TRANSRECTAL PROBE/ATL ULTRASOUND SYSTEMK911113INTERSON TRANSRECTAL PROBE/KONTRON ULTRASOUND SYSTK911117INTERSON ENDOCAVITY PROBE FOR ATL ULTRASOUND SYSTK911114INTERSON ENDOCAVITY PROBE/ALOKA ULTRASOUND SYSTEMK911464INTERSON DISPOSABLE BIOPSY NEEDLE

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Related Devices (Code: ITX)

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.

K260114Align® Cover and Pad Guidance ToolCIVCO Medical Instruments Co., Inc.K261170BA-004CCFujifilm CorporationK254143EM-TECH Passive Ultrasound Probe StrapEM-TECH Solutions, Inc.K260161SmartGuide Disposable Guides and GridsUC-CARE , Ltd.K262474ND Needle Guidance SystemAccurate Access, LLCK261014Accuro® 3S Needle Guide KitRivanna Medical, 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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