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FDA 510(k)

ELITE R/F SPOT FILM DRIVE

K-Number: K902403 · 1990-08-01

ApplicantRms Div.
Decision Date1990-08-01
Product CodeIXL
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ELITE R/F SPOT FILM DRIVE is the device name listed in this FDA 510(k) record. The listed applicant is Rms Div.. It received FDA 510(k) clearance on 1990-08-01 under 510(k) number K902403. The device is classified under product code IXL. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELITE R/F SPOT FILM DRIVE?

ELITE R/F SPOT FILM DRIVE is a medical device that received FDA 510(k) clearance on 1990-08-01. The listed applicant is Rms Div.. The 510(k) number is K902403.

When did ELITE R/F SPOT FILM DRIVE receive FDA 510(k) clearance?

ELITE R/F SPOT FILM DRIVE received FDA 510(k) clearance on 1990-08-01, under 510(k) number K902403.

Who is the listed applicant for ELITE R/F SPOT FILM DRIVE?

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

What is the FDA product code for ELITE R/F SPOT FILM DRIVE?

The FDA product code for ELITE R/F SPOT FILM DRIVE is IXL.

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Other records listing Rms Div. 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.

K963367RMS K-WIREK954438SUNMED'S GREENLINE FIBER OPTIC LARYNGOSCOPEK944848THE VIVACARE T.P.S. PROBEK944557DW250 #91K941625DW234 #29K902146SFD-035 SPOT FILM DEVICE

View all 10 devices →

Related Devices (Code: IXL)

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.

K111304OPTIMA XR120Ge Medical Systems, LLCK964806MD-1835Fischer Imaging Corp.K950317ADVANTX 1824 SPOTFILM DEVICEGE Medical SystemsK940386KODAK AUTOMIXER III INTEGRATED, KODAK AUTOMIXER III 180 LPEastman Kodak CompanyK942367AXT 1400 SPOTFILM DEVICEApplied X-Ray Technologies, Inc.K924593DIAGNOST 76 FAMILY*R/F SYSTEMS - RELEASE 4.4Philips Medical Systems, 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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