FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

DOUGLAS MEDICAL PRODUCTS, INC. IRRIGATION SET

K Number: K922318 · Decision Aug 10, 1992
Classifications
1
FEI Numbers
386
Registration Numbers
386
Same Product Code
680
Applicant Total
19
Review Days
84

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Basic Information

Device Name
DOUGLAS MEDICAL PRODUCTS, INC. IRRIGATION SET
K Number
K922318
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.1100
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Douglas Medical Products Corp.
Date Received
May 18, 1992
Decision Date
August 10, 1992
Product Code
HRX
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

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

Product Code Device Name
HRX Arthroscope

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Other Clearances by Douglas Medical Products Corp.

K Number Device Name
K961155 SOLO PICC/MIDLINE CATHETER KIT MODELS 71924, 71908
K954428 SOLOPICC 24 (60CM) 20GA CATHETER
K941628 40 MICRON BLOOD TRANSFUSION FILTER
K942101 4-LEAD IRRIGATION SET
K941453 CHECK VALVE SOLUTION SET
K930854 SOLUTION SET WITH .2 MICRON FILTER
K932637 SUBCUTANEOUS INFUSION SET
K931659 3 LEAD CONNECTOR
K931658 IN-LINE BURETTE SET
K932638 HUBER NEEDLE INFUSION SET
Search all 19 clearances from Douglas Medical Products Corp. →