Atlas FDA

OLYMPUS RIGID PERCUTANEOUS NEPHROSCOPE

FDA 510(k) clearance K853486 · decided 1985-09-12

Clearance details

K-number
K853486
Device name
OLYMPUS RIGID PERCUTANEOUS NEPHROSCOPE
Applicant
Olympus Corp.
Decision
Substantially Equivalent
Date received
1985-08-20
Decision date
1985-09-12
Days to decision
23 days
Clearance type
Traditional
Product code
FGA
Device class
2
Regulation number
876.1500
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
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
Percutaneous Nephroscope System (K232370)Karl Storz SE & CO. KG2024-05-01
Schoelly Nephroscope Set, Schoelly Ultra-Mini Nephroscope Set (K151308)Schoelly Fiberoptic GmbH2016-02-09
GYRUS ACMI IPN-2505, INVISIO SMITH PERCUTANEOUS NEPHROSCOPE SYSTEM (K072594)Gyrus Acmi, Inc.2007-12-13
NEPHROSCOPE, 12 DEGREES; DIAPHRAGM VALVE; IRRIGATION ATTACHMENT; NEPHROSCOPE, 20 DEGREE, STRAIGHT VIEW; NEPHROSCOPE, 20 (K994223)Richard Wolf Medical Instruments Corp.2000-06-05
KARL STORZ ENDOPYELOTOMY SET FOR ENDOSCOPIC UROLOGY PROCEDURES (K950433)KARL STORZ Endoscopy-America, Inc.1995-03-15
KARL STORZ ADULT & PEDIATRIC NEPHROSCOPE (K940594)KARL STORZ Endoscopy-America, Inc.1994-09-09
FLEXIBLE FIBER OPTIC ENDOSCOPE (K922826)Optimed Technologies, Inc.1993-02-19
ACMI RIGI-FLEX NEPHORSCOPE (K791182)American Cystocope Makers, Inc.1979-07-30
PYELOSCOPE SYSTEM (K770729)Richard Wolf Medical Instruments Corp.1977-04-28

Recalls involving this device

No recalls on record reference this clearance.