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

YANKAUER & POODLE SUCTION INSTRUMENTS

K Number: K790419 · Decision Apr 23, 1979
Classifications
1
FEI Numbers
174
Registration Numbers
174
Same Product Code
23
Applicant Total
16
Review Days
54

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Basic Information

Device Name
YANKAUER & POODLE SUCTION INSTRUMENTS
K Number
K790419
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6740
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Snyder Laboratories, Inc.
Date Received
February 28, 1979
Decision Date
April 23, 1979
Product Code
BYY
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
BYY Tube, Aspirating, Flexible, Connecting

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Other Clearances by Snyder Laboratories, Inc.

K Number Device Name
K843906 SNYDER HEMOVAC WOUND DRAINAGE DEVICES
K821321 SNYDER DEBRIBEMENT SYSTEM LDP-1
K800861 SNYDER HEMOVAC CHEST DRAINAGE SOLUTION
K800543 SNYDER HYSTERECTOMY Y TUBE KIT
K800577 SNYDER HEMOVAC TM VENTED WOUND KIT
K800578 SURGIVAC TM
K800542 100 ML SNYDER HEMOVAC
K790607 GREENLINE IRRIGATION TRAYS
K790606 CATHETERS, GREENLINE SUCTION
K790420 SUCTION CONNECTING TUBING
Search all 16 clearances from Snyder Laboratories, Inc. →