Britt Surgical Photocoagulator System
FDA 510(k) K837200 · Britt Corp., Inc.
510(k) numberK837200
Submission
- Device name
- Britt Surgical Photocoagulator System
- Applicant
- Britt Corp., Inc.
Hauppauge, NY, US - Received
- January 24, 1983
- Decision date
- April 4, 1983
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
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|---|---|---|
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| K974393 | Vaso Press SystemJOW · Traditional | 03/19/1999SE |
| K860977 | Model 545-45 for Neurological Surgical ApplicationLLF · Traditional | 10/16/1986SE |
| K860975 | Model 545-45 Laser for Ear, Nose & ThroatEWG · Traditional | 07/18/1986SE |
| K860974 | Model 545-45 Laser for Derma., Pod., SurgicalGEX · Traditional | 07/07/1986SE |
| K860277 | Model 525-25 Watt C02 Laser for Ear, Nose & ThroatEWG · Traditional | 05/06/1986SE |
| K860273 | Model 525 - 25 Watt CO2 Medical Laser/PodiatryGEX · Traditional | 04/23/1986SE |
| K860278 | Model 525-25 Watt CO2 Laser for Derma/PlasticGEX · Traditional | 04/15/1986SE |
| K851425 | Model J25-25 Watt CO2 LaserHHR · Traditional | 11/12/1985SE |
Questions and answers
When was Britt Surgical Photocoagulator System cleared by the FDA?
Britt Surgical Photocoagulator System (K837200) received a 510(k) decision of Substantially Equivalent on April 4, 1983, 70 days after the submission was received.