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Unistik TinyTouch Sterile Single-Use Heel Incision Safety Lancets - Preemie and Full-Term, Unistik Heelstik Sterile Single-Use Heel Incision Safety Lancets - MicroPreemie, Preemie, Full-Term and Toddler

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222168
510(k) Type
Traditional
Applicant
Owen Mumford Ltd
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
11/3/2022
Days to Decision
105 days
Submission Type
Summary

Unistik TinyTouch Sterile Single-Use Heel Incision Safety Lancets - Preemie and Full-Term, Unistik Heelstik Sterile Single-Use Heel Incision Safety Lancets - MicroPreemie, Preemie, Full-Term and Toddler

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K222168
510(k) Type
Traditional
Applicant
Owen Mumford Ltd
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
11/3/2022
Days to Decision
105 days
Submission Type
Summary