Last synced on 14 November 2025 at 11:06 pm

PENCIL POINT SPINAL NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K921683
510(k) Type
Traditional
Applicant
HART ENTERPRISES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/26/1993
Days to Decision
505 days
Submission Type
Statement

PENCIL POINT SPINAL NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K921683
510(k) Type
Traditional
Applicant
HART ENTERPRISES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/26/1993
Days to Decision
505 days
Submission Type
Statement