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11 devices found
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Manufacturer: J. Jamner Surgical Instruments, Inc.
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Jarit Endoscopes, 600-600; 600-630; 600-650; 680
J. Jamner Surgical Instruments, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K931878
Active
Cleared 19 Aug 1993
Active
510(k)
510(k)
II
Cope Lung Forceps #305-218
J. Jamner Surgical Instruments, Inc.
·
,
United States
(FDA 510(k) applicant)
Class I
FDA 510(k)
K771624
Active
Cleared 6 Sep 1977
Active
510(k)
510(k)
I
Jarit Surgical Instruments
J. Jamner Surgical Instruments, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K931959
Active
Cleared 5 Oct 1993
Active
510(k)
510(k)
II
3 variants
Jarit Surgical Instruments
K931928
Jarit Surgical Instruments
K932456
Jarit Recommended Sinus Instruments
J. Jamner Surgical Instruments, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K944670
Active
Cleared 2 Feb 1995
Active
510(k)
510(k)
II
2 variants
Jarit Recommended Sinus Instruments
K941565
Leiningeo Aortic Punch #310-395 & 397
J. Jamner Surgical Instruments, Inc.
·
,
United States
(FDA 510(k) applicant)
Class I
FDA 510(k)
K771625
Active
Cleared 12 Sep 1977
Active
510(k)
510(k)
I
Jarit Hulka Uterine Tenaculum Forceps
J. Jamner Surgical Instruments, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K082349
Active
Cleared 21 Nov 2008
Active
510(k)
510(k)
II
Jarit Surgical Instruments: Catalog 615-330, 615-331, 615-334, 615-335, 615-338, 615-339
J. Jamner Surgical Instruments, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K933728
Active
Cleared 23 Feb 1994
Active
510(k)
510(k)
II
Jarit Endoscopes, Models 600-600; 600-630; 600-650; And 600-680
J. Jamner Surgical Instruments, Inc.
·
,
United States
(FDA 510(k) applicant)
Class II
FDA 510(k)
K944870
Active
Cleared 2 Nov 1994
Active
510(k)
510(k)
II
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