Last synced on 14 November 2025 at 11:06 pm

SleeveLUX 24 Anoscope/Proctoscope (P2001); SleeveLUX 16 Anoscope/Proctoscope (P2002)

Page Type
Cleared 510(K)
510(k) Number
K250645
510(k) Type
Traditional
Applicant
Haemoband Surgical, Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
10/9/2025
Days to Decision
219 days
Submission Type
Summary

SleeveLUX 24 Anoscope/Proctoscope (P2001); SleeveLUX 16 Anoscope/Proctoscope (P2002)

Page Type
Cleared 510(K)
510(k) Number
K250645
510(k) Type
Traditional
Applicant
Haemoband Surgical, Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
10/9/2025
Days to Decision
219 days
Submission Type
Summary