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FDA 510(k)

ARRIPRO 35 ST/TV

K-Number: K973115 · 1997-09-02

ApplicantArnold & Richter Cine Technik
Decision Date1997-09-02
Product CodeIXC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ARRIPRO 35 ST/TV is the device name listed in this FDA 510(k) record. The listed applicant is Arnold & Richter Cine Technik. It received FDA 510(k) clearance on 1997-09-02 under 510(k) number K973115. The device is classified under product code IXC. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARRIPRO 35 ST/TV?

ARRIPRO 35 ST/TV is a medical device that received FDA 510(k) clearance on 1997-09-02. The listed applicant is Arnold & Richter Cine Technik. The 510(k) number is K973115.

When did ARRIPRO 35 ST/TV receive FDA 510(k) clearance?

ARRIPRO 35 ST/TV received FDA 510(k) clearance on 1997-09-02, under 510(k) number K973115.

Who is the listed applicant for ARRIPRO 35 ST/TV?

The FDA 510(k) record lists Arnold & Richter Cine Technik as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARRIPRO 35 ST/TV?

The FDA product code for ARRIPRO 35 ST/TV is IXC.

Related Clinical Trials

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Other records listing Arnold & Richter Cine Technik 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.

K993283OSCAR NET/CD, MODEL M1.82 600 . O/A/B/C

Related Devices (Code: IXC)

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.

K991302SMARTLIGHT DIGITAL FILM VIEWER, MODELS SL 4000PLUS, SL 2000PLUSSmartlight, Inc.K973965SMART MOTORIZED VIEWERSmartlight, Ltd.K970240DIFFUSER PANELFocused Viewer, Inc.K954998LILY DARK VIEWERLily Imaging Solutions Co.K954199VOXBOXVoxelK952188ADVIEWER 2000Adp , Ltd.

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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