Atlas FDA

FLEXIBLE TROCAR TUBES

FDA 510(k) clearance K930215 · decided 1993-03-16

Clearance details

K-number
K930215
Device name
FLEXIBLE TROCAR TUBES
Applicant
Olympus Corp.
Decision
Substantially Equivalent
Date received
1993-01-14
Decision date
1993-03-16
Days to decision
61 days
Clearance type
Traditional
Product code
EWY
Device class
2
Regulation number
874.4720
Medical specialty
Ear, Nose, Throat
Advisory committee
Ear, Nose, Throat
Location
Lake Success, NY, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
KARL STORZ Mediastinoscopes and Instruments (K260003)Karl Storz SE & CO. KG2026-03-02
HD Mediastinoscope (K213194)Karl Storz Endoscopy America, Inc.2022-06-23
HD Mediastinoscope (K202272)Karl Storz Endoscopy America, Inc.2021-05-11
Aegis Transit System (K170757)Boston-Biomedical Associates2017-07-14
Illuminated Mediastinal Access Port (K160171)Aegis Surgical, Ltd.2016-02-26
ILLUMINATED MEDIASTINOSCOPE (K141622)Aegis Surgical, Ltd.2015-01-09
OPTICAL MEDIASTINOSCOPE WITH PLUG-IN CONNECTION/OCULAR EYEPIECE (K971166)Richard Wolf Medical Instruments Corp.1997-08-27
KARL STORZ OPTICAL MEDIASTINOSCOPE (K954910)KARL STORZ Endoscopy-America, Inc.1995-11-03
OLYMPUS FLEXIBLE TIP THORACOSCOPE (K913829)Olympus Corp.1991-11-22
OES THORACOSCOPE SYSTEM (K912362)Olympus Corp.1991-10-24

Recalls involving this device

No recalls on record reference this clearance.