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SPINAL NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K823692
510(k) Type
Traditional
Applicant
OCEAN MEDICAL PRODUCTS, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/7/1983
Days to Decision
30 days

SPINAL NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K823692
510(k) Type
Traditional
Applicant
OCEAN MEDICAL PRODUCTS, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/7/1983
Days to Decision
30 days