Konica Srx- 701 Automatic X-Ray Film Processor
FDA 510(k) K990969 · Konica Medical Corp.
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
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| K931316 | Konica DS-7 Automatic X-Ray Film ProcessorIXW · Traditional | 12/14/1993SE |
| K931315 | Konica SRX-501A Automatic X-Ray Film ProcessorIXW · Traditional | 12/14/1993SE |
| K931314 | Konica QX-70 Automatic X-Ray Film ProcessorIXW · Traditional | 09/07/1993SE |
| K931313 | Konica QX-130APLUS Automatic X-Ray Film ProcessorIXW · Traditional | 09/07/1993SE |
| K931312 | Konica SRX-101 Automatic X-Ray Film ProcessorIXW · Traditional | 09/07/1993SE |
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.