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

MEDI-PUMP

K Number: K944399 · Decision Jan 18, 1995
Classifications
1
FEI Numbers
98
Registration Numbers
98
Same Product Code
158
Applicant Total
9
Review Days
132

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Basic Information

Device Name
MEDI-PUMP
K Number
K944399
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4780
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Thomas Industries
Date Received
September 8, 1994
Decision Date
January 18, 1995
Product Code
BTA
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
BTA Pump, Portable, Aspiration (Manual Or Powered)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (BTA), ordered by most recent decision date.

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Other Clearances by Thomas Industries

K Number Device Name
K041199 MEDI-PUMP ASPIRATOR, MODEL 1615
K965059 CPI, MAXI-VAC(6480),THOMAS INDUSTRIES, MEDI-PUMP(1240/1242/1243)
K952806 MEDI PUMP ASPIRATOR MODELS 1130 AND 1135
K950290 MEDI - PUMP
K951729 MEDI - PUMP
K950867 MEDI - PUMP
K925010 NEBULIZER PUMP, POWERED, MODEL 1110
K925011 NEBULIZER PUMP, POWERED MODEL 1180