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FDA 510(k)

INTERSON DISPOSABLE BIOPSY NEEDLE

K-Number: K911464 · 1991-09-27

ApplicantInterson Corp.
Decision Date1991-09-27
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

INTERSON DISPOSABLE BIOPSY NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Interson Corp.. It received FDA 510(k) clearance on 1991-09-27 under 510(k) number K911464. 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 INTERSON DISPOSABLE BIOPSY NEEDLE?

INTERSON DISPOSABLE BIOPSY NEEDLE is a medical device that received FDA 510(k) clearance on 1991-09-27. The listed applicant is Interson Corp.. The 510(k) number is K911464.

When did INTERSON DISPOSABLE BIOPSY NEEDLE receive FDA 510(k) clearance?

INTERSON DISPOSABLE BIOPSY NEEDLE received FDA 510(k) clearance on 1991-09-27, under 510(k) number K911464.

Who is the listed applicant for INTERSON DISPOSABLE BIOPSY NEEDLE?

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 DISPOSABLE BIOPSY NEEDLE?

The FDA product code for INTERSON DISPOSABLE BIOPSY NEEDLE is IYO.

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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 SYSTK911113INTERSON TRANSRECTAL PROBE/KONTRON ULTRASOUND SYSTK911115INTERSON TRANSRECTAL PROBE/ATL ULTRASOUND SYSTEMK911117INTERSON ENDOCAVITY PROBE FOR ATL ULTRASOUND SYSTK911114INTERSON ENDOCAVITY PROBE/ALOKA ULTRASOUND SYSTEMK900555INTERSON MULTIPLANE RECTAL PROBE FOR ALOKA ULTRA.

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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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