Metatech Metal Microclip
FDA 510(k) K881447 · Metatech Corp.
510(k) numberK881447
Submission
- Device name
- Metatech Metal Microclip
- Applicant
- Metatech Corp.
Pittsburgh, PA, US - Received
- April 6, 1988
- Decision date
- June 22, 1988
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- DXC – Clamp, Vascular
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.4450
- Specialty
- Cardiovascular
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| K883881 | Modified Model 2001 Fiber Optics CatheterGWM · Traditional | 10/27/1988SE |
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Questions and answers
When was Metatech Metal Microclip cleared by the FDA?
Metatech Metal Microclip (K881447) received a 510(k) decision of Substantially Equivalent on June 22, 1988, 77 days after the submission was received.
What is the product code of K881447?
The FDA product code is DXC – Clamp, Vascular, a Class II (moderate risk) device regulated under 21 CFR 870.4450.