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

CAT.#40100, 40102, 40104 & 40106 YANKAUER SUCT INT

K Number: K921464 · Decision May 5, 1992
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
7
Applicant Total
44
Review Days
39

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Basic Information

Device Name
CAT.#40100, 40102, 40104 & 40106 YANKAUER SUCT INT
K Number
K921464
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4200
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Trinity Laboratories, Inc.
Date Received
March 27, 1992
Decision Date
May 5, 1992
Product Code
GBQ
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
GBQ Catheter, Continuous Irrigation

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K974286 CIRCUMCISION TRAY, CAT. NO. 70340
K972160 CRP-LEX SYSTEM: C-REACTIVE PROTEIN ANTIGEN DETECTION IN SERUM: SLIDE AGGLUTNATION LATEX TEST
K970722 EYE TRAY
K965201 O.R. SCRUB PREP TRAY, STERILE, DISPOSABLE
K964921 BASIC BIOPSY TRAY. DISPOSABLE, STERILE
K953929 MID-STREAM COLLECTION SET-STERILE
K952058 STERILE V.A.D. (VASCULAR ACCESS DEVICES) ACCESS KIT, DISPOSABLE
K953070 WOUNDFOAM 4 X 4
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