FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

Lancing device (HH-XV-T)

K Number: K253706 · Decision Dec 9, 2025
Classifications
1
FEI Numbers
84
Registration Numbers
84
Same Product Code
23
Applicant Total
12
Review Days
15

Basic Information

Device Name
Lancing device (HH-XV-T)
K Number
K253706
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.4850
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Tianjin Huahong Technology Co., Ltd.
Date Received
November 24, 2025
Decision Date
December 9, 2025
Product Code
QRL
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
QRL Multiple Use Blood Lancet For Single Patient Use Only

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (QRL), ordered by most recent decision date.

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Other Clearances by Tianjin Huahong Technology Co., Ltd.

K Number Device Name
K260191 Safety lancet (XXXVII)
K252490 Heel Stick Safety Lancet (HHZ-II, HHZ-III, HHZ-IV)
K251694 safety lancet
K243306 Lancet (IA, IB, IC, ID, IE, IK, IL, IM, IIA, IIB, III, V, VI, VII, VIII, IX); Lancing device (HH-X-T, HH-XV-T, HH-XVI-T, HH-XVII-T, HH-XVIII-T, HH-XIX, HH-XXI-T, HH-XXII-T, HH-XXIII-T, HH-XXIV-T, HH-XXV-T, HH-XXVI-T, HH-XXVIII-T, HH-XXIX-T, HH-XXX-T, HH-XIII-T, HH-XXVII-T)
K241627 Safety Lancet (XXXV)
K240806 Safety lancet (XXVIII, XXIX, XXX, XXXI, XXXII, XXXIII, XXXIV.)
K220475 Lancet (I, II, III, V, VI); Lancing device (HH-X-T, HH-XIII-T, HH-XV-T, HH-XVI-T, HH-XVII-T, HH-XVIII-T, HH-XIX, HH-XXI-T, HH-XXII-T, HH-XXIII-T, HH-XXIV-T)
K221176 Insulin Pen Needle
K220370 Safety Lancet (XIII, XVII, XXI, XXII, XXIII, XXIV, XXV, XXVI)
K220372 Heel Stick Safety Lancet (HHZ-II, HHZ-III)
Search all 12 clearances from Tianjin Huahong Technology Co., Ltd. →