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

MID-STREAM COLLECTION SET-STERILE

K Number: K953929 · Decision Nov 16, 1995
Classifications
1
FEI Numbers
45
Registration Numbers
45
Same Product Code
62
Applicant Total
44
Review Days
87

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Basic Information

Device Name
MID-STREAM COLLECTION SET-STERILE
K Number
K953929
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2900
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Trinity Laboratories, Inc.
Date Received
August 21, 1995
Decision Date
November 16, 1995
Product Code
LIO
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

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

Product Code Device Name
LIO Device, Specimen Collection

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Other Clearances by Trinity Laboratories, Inc.

K Number Device Name
K981441 HEART CATH TRAY, STERILE, DISPOSABLE
K974238 DENTAL TRAY, STERILE, DISPOSABLE
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
K952058 STERILE V.A.D. (VASCULAR ACCESS DEVICES) ACCESS KIT, DISPOSABLE
K953070 WOUNDFOAM 4 X 4
K951506 SUCTION CATHETER KIT, STERILE, SINGLE-USE
Search all 44 clearances from Trinity Laboratories, Inc. →