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

NK MEDICAL MICROMETER, MODEL MC001

K Number: K921266 · Decision Jul 14, 1992
Classifications
1
FEI Numbers
194
Registration Numbers
194
Same Product Code
6
Applicant Total
15
Review Days
120

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
NK MEDICAL MICROMETER, MODEL MC001
K Number
K921266
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
888.4150
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Nk Biotechnical Engineering Co.
Date Received
March 16, 1992
Decision Date
July 14, 1992
Product Code
KTZ
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

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

Product Code Device Name
KTZ Caliper

Similar 510(k) Clearances

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

View all

Other Clearances by Nk Biotechnical Engineering Co.

K Number Device Name
K934368 NK PRESSURE-SPECIFIED SENSORY DEVICE, MODEL PSSD-001
K923964 NK GRASP SENSOR, MODEL GA001
K923965 NK GRASP SENSOR, MODEL GA002
K923963 NK DIGI-GRIP SENSOR, MODEL DGR001
K921268 NK DYNA-GRIP SENSOR, MODEL DG001
K914057 NK PINCH SENSOR, MODEL PA001
K914061 NK RANGE OF MOTION SENSOR, MODEL RM002
K914056 NK PINCH SENSOR, MODEL PF002
K914062 NK DEXTERITLY BOARD, MODEL BX001
K914059 NK DEVIATION SENSOR, MODEL DV001
Search all 15 clearances from Nk Biotechnical Engineering Co. →