Latex Penrose Tubing
FDA 510(k) K822755 · American Hospital Supply Corp.
510(k) numberK822755
Submission
- Device name
- Latex Penrose Tubing
- Applicant
- American Hospital Supply Corp.
Mchenry, IL, US - Received
- September 8, 1982
- Decision date
- January 21, 1983
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
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|---|---|---|
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| K822990 | Convertors Primary Wound Dressing IIFRO · Traditional | 04/12/1983SE |
| K830343 | Container W/Priming SolutionKDP · Traditional | 03/17/1983SE |
| K830301 | Stratus Fluorometric Enzyme IMMUN0-JJE · Traditional | 02/25/1983SE |
| K823418 | Heyer-Schute Universal Ureteral StentLJE · Traditional | 12/03/1982SE |
| K822966 | Convertors Disposable Dressing SpongeNAB · Traditional | 11/05/1982SE |
| K822754 | Ear/Ulcer SyringeKCP · Traditional | 10/04/1982SE |
Questions and answers
When was Latex Penrose Tubing cleared by the FDA?
Latex Penrose Tubing (K822755) received a 510(k) decision of Substantially Equivalent on January 21, 1983, 135 days after the submission was received.