ENDOPOUCH PRO SPECIMEN RETRIEVAL BAG— 510(k) K981579
Substantially EquivalentETHICON, Inc.
FDA 510(k) clearance K981579 for ENDOPOUCH PRO SPECIMEN RETRIEVAL BAG, Substantially Equivalent on 1998-07-09. Applicant: ETHICON, Inc.. Device class: 1.
Clearance details
- Applicant
- ETHICON, Inc.
- Product code
- Code MDM
- Device class
- Class 1
- Regulation
- 21 CFR 878.4800
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Somerville, NJ, US
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Adverse events under product code MDM
product code MDM- Injury
- 247
- Malfunction
- 1,516
- Total
- 1,763
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.