Sony PVM-2551MD Oled Monitor

FDA 510(k) K120611 · Sony Electronics, Inc.

Substantially Equivalent

510(k) numberK120611

Submission

Device name
Sony PVM-2551MD Oled Monitor
Applicant
Sony Electronics, Inc.
North Attleboro, MA, US
Received
February 29, 2012
Decision date
June 28, 2012
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
GCJ – Laparoscope, General & Plastic Surgery
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Specialty
Gastroenterology, Urology

Validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission if the device is reusable and has specific design features (please refer to Table 2 of 82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).

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Questions and answers

When was Sony PVM-2551MD Oled Monitor cleared by the FDA?

Sony PVM-2551MD Oled Monitor (K120611) received a 510(k) decision of Substantially Equivalent on June 28, 2012, 120 days after the submission was received.

What is the product code of K120611?

The FDA product code is GCJ – Laparoscope, General & Plastic Surgery, a Class II (moderate risk) device regulated under 21 CFR 876.1500.