Konica Srx- 701 Automatic X-Ray Film Processor

FDA 510(k) K990969 · Konica Medical Corp.

Substantially Equivalent

510(k) numberK990969

Submission

Device name
Konica Srx- 701 Automatic X-Ray Film Processor
Applicant
Konica Medical Corp.
New York, NY, US
Received
March 23, 1999
Decision date
June 18, 1999
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
IXW – Processor, Radiographic-Film, Automatic
Device class
Class II (moderate risk)
Regulation
21 CFR 892.1900
Specialty
Radiology

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Questions and answers

When was Konica Srx- 701 Automatic X-Ray Film Processor cleared by the FDA?

Konica Srx- 701 Automatic X-Ray Film Processor (K990969) received a 510(k) decision of Substantially Equivalent on June 18, 1999, 87 days after the submission was received.

What is the product code of K990969?

The FDA product code is IXW – Processor, Radiographic-Film, Automatic, a Class II (moderate risk) device regulated under 21 CFR 892.1900.