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

CATHETERS, GREENLINE SUCTION

K Number: K790606 · Decision Apr 23, 1979
Classifications
1
FEI Numbers
245
Registration Numbers
245
Same Product Code
115
Applicant Total
16
Review Days
25

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Basic Information

Device Name
CATHETERS, GREENLINE SUCTION
K Number
K790606
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.6810
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Snyder Laboratories, Inc.
Date Received
March 29, 1979
Decision Date
April 23, 1979
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 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
K790420 SUCTION CONNECTING TUBING
K790419 YANKAUER & POODLE SUCTION INSTRUMENTS
Search all 16 clearances from Snyder Laboratories, Inc. →