FIBER OPTIC ADAPTER #60-0896— 510(k) K802775

Name: FDA 510(k) clearance K802775
Creator: U.S. Food and Drug Administration
Published: 1980-12-16

Substantially Equivalent

Aspen Laboratories, Inc.

FDA 510(k) clearance K802775 for FIBER OPTIC ADAPTER #60-0896, Substantially Equivalent on 1980-12-16. Applicant: Aspen Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Aspen Laboratories, Inc.
Product code: Code EQH
Device class: Class 1
Regulation: 21 CFR 874.4350
Advisory panel: Ear, Nose, Throat
Date received: 1980-11-03
Decision date: 1980-12-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: MD, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EQH

view all

K945876 — WECO ENDOSCOPIC SYSTEM WITH FIBER OPTIC LIGHT1995-12-04
K954184 — JED-LIGHT FIBEROPTIC LIGHT SOURCE1995-11-13
K951829 — COLD LIGHT SOURCE LOS 1501995-07-10
K932771 — BATTERY POWERED, DISPOSABLE ENDOSCOPE LIGHT SOURCE1994-08-24
K941661 — GM OPTI*CAM CAMER WITH DENTAL FIBER OPTIC LIGHT1994-08-23

More clearances from Aspen Laboratories, Inc.

view all

K981220 — SYSTEM 7500 ABC ELECTROSURGICAL UNIT1998-04-21
K963088 — SHEATH, ELECTROSURGICAL PENCIL1996-09-13
K955834 — SYSTEM 6500 ABC ELECTROSURGICAL UNIT1996-07-11
K960296 — 4000 ETM1996-02-20
K953081 — BEAMER PLUS1995-10-30

Data sourced from openFDA. This site is unofficial and independent of the FDA.