Hollister Male Urinary Incont. System
FDA 510(k) K810708 · Hollister, Inc.
510(k) numberK810708
Submission
- Device name
- Hollister Male Urinary Incont. System
- Applicant
- Hollister, Inc.
Walker, MI, US - Received
- March 17, 1981
- Decision date
- March 17, 1981
- Decision
- Unknown (SESP)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
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|---|---|---|
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| K233524 | Sleeved IC 2 Family; Sleeved IC 2 SWT (Name not Finalized); Sleeved IC 2 Plus (Name not…EZD · Traditional | 05/03/2024SE |
| K220667 | Sleeved ICEZD · Traditional | 12/08/2022SE |
| K213575 | Female IC (Not Finalized)EZD · Traditional | 09/13/2022SE |
| K211436 | Intermittent Catheter (Not Finalized)GBM · Traditional | 01/27/2022SE |
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| K183253 | ValPro 2 Plus, VaPro 2 Plus PocketGBM · Special | 12/18/2018SE |
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Questions and answers
When was Hollister Male Urinary Incont. System cleared by the FDA?
Hollister Male Urinary Incont. System (K810708) received a 510(k) decision of Unknown on March 17, 1981, 0 days after the submission was received.