Codman Laser Neuroendoscope
FDA 510(k) K924977 · Codman & Shurtleff, Inc.
510(k) numberK924977
Submission
- Device name
- Codman Laser Neuroendoscope
- Applicant
- Codman & Shurtleff, Inc.
Randolph, MA, US - Received
- October 1, 1992
- Decision date
- November 22, 1993
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- GWG – Endoscope, Neurological
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 882.1480
- Specialty
- Neurology
If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (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 Codman Laser Neuroendoscope cleared by the FDA?
Codman Laser Neuroendoscope (K924977) received a 510(k) decision of Substantially Equivalent on November 22, 1993, 417 days after the submission was received.
What is the product code of K924977?
The FDA product code is GWG – Endoscope, Neurological, a Class II (moderate risk) device regulated under 21 CFR 882.1480.