Imm Enterprises , Ltd. - FDA 510(k) Cleared Devices
52
Total
52
Cleared
0
Denied
Imm Enterprises , Ltd. has 52 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 52 cleared submissions from 1983 to 1984. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Imm Enterprises , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Imm Enterprises , Ltd.
52 devices
Cleared
May 09, 1984
CAT. 7-EAR, NOSE & THROAT DEVICES
Ear, Nose, Throat
106d
Cleared
May 09, 1984
KOLLMANN URETHRAL DILATOR
Gastroenterology & Urology
43d
Cleared
May 09, 1984
WESTON RECTAL SNARE
Gastroenterology & Urology
43d
Cleared
May 01, 1984
CATEGORY 17-MICROBIOLOGY DEVICES
General & Plastic Surgery
98d
Cleared
Apr 23, 1984
CATEGORY 1 CIRCULATORY SYSTEM DEVICE
Cardiovascular
90d
Cleared
Apr 23, 1984
CAT. 14-CLINICAL TOXIOLOGY DEVICES
General & Plastic Surgery
90d
Cleared
Apr 05, 1984
CAT. 8 DENTAL DEVICES
Dental
72d
Cleared
Apr 04, 1984
OP-CON SURG. INSTRUMENT #3
Gastroenterology & Urology
135d
Cleared
Mar 22, 1984
JAKOBI SURGICAL INSTRUMENTS #3 17/18/19
Gastroenterology & Urology
122d
Cleared
Mar 22, 1984
JAKOBI SURG. INSTRUMENTS #3 21/22/24
Gastroenterology & Urology
122d
Cleared
Mar 16, 1984
CATEGORY 6 OPTHALMIC DEVICES
Ophthalmic
52d
Cleared
Mar 12, 1984
CATEGORY 2 GEN. HOSPITAL & PERSONAL USE
General & Plastic Surgery
48d
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