MOBLVAC III— 510(k) K933902
Substantially EquivalentAeros Instruments, Inc.
FDA 510(k) clearance K933902 for MOBLVAC III, Substantially Equivalent on 1994-05-20. Applicant: Aeros Instruments, Inc.. Device class: 2.
Clearance details
- Applicant
- Aeros Instruments, Inc.
- Product code
- Code BTA
- Device class
- Class 2
- Regulation
- 21 CFR 878.4780
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Northbrook, IL, US
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More clearances from Aeros Instruments, Inc.
view allAdverse events under product code BTA
product code BTA- Death
- 5
- Total
- 5
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 →
Recalls naming K933902
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K933902.
Data sourced from openFDA. This site is unofficial and independent of the FDA.