Last synced on 14 November 2025 at 11:06 pm

MEROCEL MEROSPLINT

Page Type
Cleared 510(K)
510(k) Number
K933152
510(k) Type
Traditional
Applicant
MEROCEL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/17/1993
Days to Decision
49 days
Submission Type
Statement

MEROCEL MEROSPLINT

Page Type
Cleared 510(K)
510(k) Number
K933152
510(k) Type
Traditional
Applicant
MEROCEL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/17/1993
Days to Decision
49 days
Submission Type
Statement