Triangular Jaw Microlaryngeal Forceps
FDA 510(k) K925370 · Pilling Co.
510(k) numberK925370
Submission
- Device name
- Triangular Jaw Microlaryngeal Forceps
- Applicant
- Pilling Co.
Fort Washington, PA, US - Received
- October 23, 1992
- Decision date
- March 18, 1993
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
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| K925198 | Kaiser No Cannula Thoracoscopy/Laparoscopy InstrGCJ · Traditional | 02/12/1993SE |
| K922971 | No-Scalpel Vascetomy InstrumentsKOA · Traditional | 09/23/1992SE |
| K914015 | Clement-Pilling Cholangiography Cath Guide/ClampGBZ · Traditional | 11/21/1991SE |
| K911099 | Mehigan-Pilling Angioscopic Vascular Instrum. LineDWX · Traditional | 06/25/1991SE |
| K911100 | Mehigan-Pilling Phlebetome TMMGZ · Traditional | 06/21/1991SE |
| K904507 | Pilling Brush ValvulotomeDWQ · Traditional | 03/01/1991SE |
| K884946 | Jehle Coronary Perfusion CathetersKRA · Traditional | 02/06/1989SE |
| K882930 | Laser Laryngoscope Dedo Articula. & Feder Dedo ExCCW · Traditional | 08/16/1988SE |
Questions and answers
When was Triangular Jaw Microlaryngeal Forceps cleared by the FDA?
Triangular Jaw Microlaryngeal Forceps (K925370) received a 510(k) decision of Substantially Equivalent on March 18, 1993, 146 days after the submission was received.
What is the product code of K925370?
The FDA product code is ELW – Material, Impression, a Class II (moderate risk) device regulated under 21 CFR 872.3660.