Last synced on 14 November 2025 at 11:06 pm

AMNIO CENTESES KIT W/NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K830019
510(k) Type
Traditional
Applicant
UNIVERSAL MEDICAL INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/1983
Days to Decision
14 days

AMNIO CENTESES KIT W/NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K830019
510(k) Type
Traditional
Applicant
UNIVERSAL MEDICAL INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/1983
Days to Decision
14 days