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

VANISHPOINT SYRINGE

K Number: K980069 · Decision Feb 12, 1998
Classifications
1
FEI Numbers
143
Registration Numbers
143
Same Product Code
163
Applicant Total
12
Review Days
35

Basic Information

Device Name
VANISHPOINT SYRINGE
K Number
K980069
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5860
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
RETRACTABLE TECHNOLOGIES, INC.
Date Received
January 8, 1998
Decision Date
February 12, 1998
Product Code
MEG
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
MEG Syringe, Antistick

Similar 510(k) Clearances

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Other Clearances by RETRACTABLE TECHNOLOGIES, INC.

K Number Device Name
K133635 EASYPOINT NEEDLE
K122355 VANISHPOINT BLOOD COLLECTION SET
K112512 VANISHPOINT BLOOD COLLECTION SET
K101708 PATIENT SAFE LUER CAP
K081420 VANISHPOINT I.V. CATHETER
K072654 PATIENT SAFE SYRINGE
K051355 VANISHPOINT I.V. CATHETER
K973301 ANTI-STICK SYRINGE WITH INTEGRAL HYPODERMIC NEEDLE/VANISHPOINT SYRINGE
K971763 BLOOD COLLECTION TUBE HOLDER VANISHPOINT TUBE HOLDER/SMALL TUBE ADAPTER
K970803 ANTI-STICK SYRINGE WITH INTEGRAL HYPODERMIC NEEDLE VANISHPOINT SYRINGE
Search all 12 clearances from RETRACTABLE TECHNOLOGIES, INC. →