Ksea Set for Endoscopic Assisted Intubation

FDA 510(k) K962393 · KARL STORZ Endoscopy-America, Inc.

Substantially Equivalent

510(k) numberK962393

Submission

Device name
Ksea Set for Endoscopic Assisted Intubation
Applicant
KARL STORZ Endoscopy-America, Inc.
Culver City, CA, US
Received
June 20, 1996
Decision date
September 17, 1996
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
GCM – Endoscope, Rigid
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Specialty
Gastroenterology, Urology

Other 510(k)s with product code GCM

510(k)DeviceApplicantDecision
K203226Telescope 0 O 10MM WL 305MM / Telescope 30 O 10MM WL 305MM / Telescope 50 O 10MM WL…GCM · Traditional Richard Wolf Medical Instruments Corporation05/14/2021SE
K083840Msi Medserv International-Rigid EndoscopeGCM · Traditional Msi Medserv International Deutschland GmbH09/28/2009SE
K001217Inside ViewGCM · Traditional Monadnock Optics, Inc.07/11/2000SE
K993103ENDOSCOPES,10MM Diameter 0 Degrees; Endoscopes, 10MM Diameter, 30 Degrees; Endoscopes…GCM · Traditional Richard Wolf Medical Instruments Corp.12/10/1999SE
K993445Omnisonic Endoscopic DeflectorGCM · Traditional Omnisonics Medical Technologies12/06/1999SE
K950712Portable Endoscopy SystemGCM · Traditional Laser-Optik-Systeme GmbH & Co. KG05/14/1996SE
K955120Hand-Held Retractor, Dissector & DissectorGCM · Traditional Ethicon Endo-Surgery, Inc.01/26/1996SE
K935235Endoscopy System for Facial Plastic SurgeryGCM · Traditional Smith & Nephew Richards, Inc.03/23/1995SE
K945889Karl Storz Plastic Surgery AccessoriesGCM · Traditional KARL STORZ Endoscopy-America, Inc.03/22/1995SE
K931954Thoracoscope/LaparoscopeGCM · Traditional Surgical Technologies, Inc.11/02/1993SE

More from Surgical Technologies, Inc.

510(k)DeviceDecision
K252624KARL STORZ Laryngoscopes and AccessoriesEQN · Traditional 05/15/2026SE
K240506KARL STORZ HoldersOCV · Traditional 10/22/2024SE
K223885HOPKINS TelescopesHIH · Traditional 09/14/2023SE
K230359KOH Ultramicro Injection Cannula (26167NN); Suction a. Irrig. Cannula,L. 36cm (37360CP)…GCJ · Traditional 06/23/2023SE
K223520UNIDRIVE SIII SystemHIH · Traditional 04/27/2023SE
K223923HOPKINS TelescopesGCJ · Traditional 03/30/2023SE
K221893KARL STORZ Bipolar Resectoscopes with HF CableFJL · Traditional 03/17/2023SE
K221004HOPKINS TelescopesGCJ · Traditional 12/20/2022SE
K222504H1GCJ · Traditional 11/10/2022SE
K213194HD MediastinoscopeEWY · Traditional 06/23/2022SE

Questions and answers

When was Ksea Set for Endoscopic Assisted Intubation cleared by the FDA?

Ksea Set for Endoscopic Assisted Intubation (K962393) received a 510(k) decision of Substantially Equivalent on September 17, 1996, 89 days after the submission was received.

What is the product code of K962393?

The FDA product code is GCM – Endoscope, Rigid, a Class II (moderate risk) device regulated under 21 CFR 876.1500.