FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

CATEGORY 1 CIRCULATORY SYSTEM DEVICE

K Number: K840305 · Decision Apr 23, 1984
Classifications
1
FEI Numbers
313
Registration Numbers
313
Same Product Code
70
Applicant Total
52
Review Days
90

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Basic Information

Device Name
CATEGORY 1 CIRCULATORY SYSTEM DEVICE
K Number
K840305
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
870.4500
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Imm Enterprises , Ltd.
Date Received
January 24, 1984
Decision Date
April 23, 1984
Product Code
DWS
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DWS Instruments, Surgical, Cardiovascular

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Other Clearances by Imm Enterprises , Ltd.

K Number Device Name
K840311 CAT. 7-EAR, NOSE & THROAT DEVICES
K841387 WESTON RECTAL SNARE
K841386 KOLLMANN URETHRAL DILATOR
K840304 CATEGORY 17-MICROBIOLOGY DEVICES
K840318 CAT. 14-CLINICAL TOXIOLOGY DEVICES
K840312 CAT. 8 DENTAL DEVICES
K834171 OP-CON SURG. INSTRUMENT #3
K834191 JAKOBI SURGICAL INSTRUMENTS #3 17/18/19
K834192 JAKOBI SURG. INSTRUMENTS #3 21/22/24
K840310 CATEGORY 6 OPTHALMIC DEVICES
Search all 52 clearances from Imm Enterprises , Ltd. →