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

MECONIUM ASPIRATOR

K Number: K871407 · Decision Jun 15, 1987
Classifications
1
FEI Numbers
245
Registration Numbers
245
Same Product Code
115
Applicant Total
29
Review Days
68

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Basic Information

Device Name
MECONIUM ASPIRATOR
K Number
K871407
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.6810
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Intertech Resources, Inc.
Date Received
April 8, 1987
Decision Date
June 15, 1987
Product Code
BSY
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
BSY Catheters, Suction, Tracheobronchial

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Other Clearances by Intertech Resources, Inc.

K Number Device Name
K961318 1ST RESPONSE DISPOSABLE MANOMETER
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K953580 HEAT MOISTURE EXCHANGER
K952223 XENON GAS BREATHING CIRCUIT
K952062 PFT FILTER
K952169 SAFE RESPONSE MOUTH-TO-MASK RESUSCITATOR, PEDIATRIC
K952214 SIMS INTERTECH HYPERINFLATION BAG SYSTEM
K935036 HEPA FILTERED HEAT AND MOISTURE EXCHANGER
K930816 HEPA FILTERED HME
K922479 DISPOSABLE ANESTHESIA BREATHING CIRCUIT, MODIFIED
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