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Product codes
GCL
Product code GCL
Device name
Esophagoscope, General & Plastic Surgery
Medical specialty
Gastroenterology, Urology
Device class
2
Regulation number
876.1500
Review panel
GU
Implant
N
Life sustaining/supporting
N
GMP exempt
N
Third party review
N
Summary malfunction reporting
Ineligible
Definition
If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).
Source
FDA openFDA device classification dataset
Related 510(k) Records
#
510(k), Device, Applicant table
510(k)
Device
Applicant
Decision date
K951197
FE-24X, FIBER ESOPHAGOSCOPE
Pentax Precision Instrument Corp.
1995-05-30
K951198
FE-34TH, FIBER ESOPHAGOSCOPE
Pentax Precision Instrument Corp.
1995-05-30
K934510
5,6,7,9,10,11,12MM BLUNT-TIP TROCAR OBTUR/THREAD
Phx Technologies Corp.
1994-02-17
K922086
BARD BIOPSY FORCEPS
C.R. Bard, Inc.
1992-10-30
Related GUDID Devices
#
Primary DI, Brand, Company table
Primary DI
Brand
Company
Published
16971381251613
Single-use Biopsy Forceps
SCIVITA MEDICAL TECHNOLOGY CO., LTD.
2023-05-24
00812608021581
PMI
PROGRESSIVE MEDICAL, INC.
2017-10-04
10812608021588
PMI
PROGRESSIVE MEDICAL, INC.
2017-10-04
04961333224722
PENTAX
HOYA CORPORATION
2017-04-07
04961333224746
PENTAX
HOYA CORPORATION
2017-04-07
04961333224784
PENTAX
HOYA CORPORATION
2017-04-07
04961333224807
PENTAX
HOYA CORPORATION
2017-04-07
04961333227471
PENTAX
HOYA CORPORATION
2017-04-07
04961333227495
PENTAX
HOYA CORPORATION
2017-04-07
04961333227518
PENTAX
HOYA CORPORATION
2017-04-07
04961333227532
PENTAX
HOYA CORPORATION
2017-04-07
04961333232741
FIBER ESOPHAGOSCOPE
PENTAX OF AMERICA, INC.
2017-04-06
00812608021314
PMI
PROGRESSIVE MEDICAL, INC.
2016-09-23
00812608021376
PMI
PROGRESSIVE MEDICAL, INC.
2016-09-23