Sponge System, Rosering Contain-Count
FDA 510(k) K782120 · Medline Industries, Inc.
510(k) numberK782120
Submission
- Device name
- Sponge System, Rosering Contain-Count
- Applicant
- Medline Industries, Inc.
Mchenry, IL, US - Received
- December 27, 1978
- Decision date
- December 27, 1978
- Decision
- Unknown (SESP)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
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Questions and answers
When was Sponge System, Rosering Contain-Count cleared by the FDA?
Sponge System, Rosering Contain-Count (K782120) received a 510(k) decision of Unknown on December 27, 1978, 0 days after the submission was received.