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

Safety lancet (XXXVII)

K Number: K260191 · Decision Mar 31, 2026
Classifications
1
FEI Numbers
157
Registration Numbers
157
Same Product Code
109
Applicant Total
12
Review Days
68

Basic Information

Device Name
Safety lancet (XXXVII)
K Number
K260191
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4850
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Tianjin Huahong Technology Co., Ltd.
Date Received
January 22, 2026
Decision Date
March 31, 2026
Product Code
FMK
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
FMK Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature

Similar 510(k) Clearances

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

View all

Other Clearances by Tianjin Huahong Technology Co., Ltd.

K Number Device Name
K252490 Heel Stick Safety Lancet (HHZ-II, HHZ-III, HHZ-IV)
K253706 Lancing device (HH-XV-T)
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. →