Unimax Specimen Retrieval System
FDA 510(k) K103510 · Unimax Medical Systems, Inc.
510(k) numberK103510
Submission
- Device name
- Unimax Specimen Retrieval System
- Applicant
- Unimax Medical Systems, Inc.
Taipei County, TW - Received
- November 29, 2010
- Decision date
- May 6, 2011
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- GCJ – Laparoscope, General & Plastic Surgery
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 876.1500
- Specialty
- Gastroenterology, Urology
Validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission if the device is reusable and has specific design features (please refer to Table 2 of 82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).
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Questions and answers
When was Unimax Specimen Retrieval System cleared by the FDA?
Unimax Specimen Retrieval System (K103510) received a 510(k) decision of Substantially Equivalent on May 6, 2011, 158 days after the submission was received.
What is the product code of K103510?
The FDA product code is GCJ – Laparoscope, General & Plastic Surgery, a Class II (moderate risk) device regulated under 21 CFR 876.1500.