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510(k) K001217

INSIDE VIEW by Monadnock Optics, Inc. — Product Code GCM

K001217 is an FDA 510(k) premarket notification submitted by Monadnock Optics, Inc. for the device "INSIDE VIEW". The FDA issued a decision of Substantially Equivalent on July 11, 2000. The device falls under product code GCM (Endoscope, Rigid), a Class II device regulated under 21 CFR 876.1500.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 11, 2000
Date Received
April 17, 2000
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Endoscope, Rigid
Device Class
Class II
Regulation Number
876.1500
Review Panel
GU
Submission Type

Other clearances for product code GCM

  • K203226 — TELESCOPE 0 O 10MM WL 305MM / TELESCOPE 30 O 10MM WL 305MM / TELESCOPE 50 O 10MM (May 14, 2021)
  • K083840 — MSI MEDSERV INTERNATIONAL-RIGID ENDOSCOPE (September 28, 2009)
  • K993103 — ENDOSCOPES,10MM DIAMETER 0 DEGREES; ENDOSCOPES, 10MM DIAMETER, 30 DEGREES; ENDOS (December 10, 1999)
  • K993445 — OMNISONIC ENDOSCOPIC DEFLECTOR (December 6, 1999)
  • K962393 — KSEA SET FOR ENDOSCOPIC ASSISTED INTUBATION (September 17, 1996)
  • K950712 — PORTABLE ENDOSCOPY SYSTEM (May 14, 1996)
  • K955120 — HAND-HELD RETRACTOR, DISSECTOR & DISSECTOR (January 26, 1996)
  • K935235 — ENDOSCOPY SYSTEM FOR FACIAL PLASTIC SURGERY (March 23, 1995)
  • K945889 — KARL STORZ PLASTIC SURGERY ACCESSORIES (March 22, 1995)
  • K931954 — THORACOSCOPE/LAPAROSCOPE (November 2, 1993)

FDA data resources