ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER MS822— 510(k) K980224
Substantially EquivalentAlexander Mfg. Co.
FDA 510(k) clearance K980224 for ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER MS822, Substantially Equivalent on 1998-04-02. Applicant: Alexander Mfg. Co.. Device class: 1.
Clearance details
- Applicant
- Alexander Mfg. Co.
- Product code
- Code MOQ
- Device class
- Class 1
- Regulation
- 21 CFR 878.4820
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mason City, IA, US
Recent devices under product code MOQ
view allMore clearances from Alexander Mfg. Co.
view all- K982896 — ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER LP9
- K981776 — ALEXANDER MANUFACTURING CO. BATTERY PART NUMBER MC146X
- K981728 — ALEXANDER MANUFACTURING CO. BATTERY PART NUMBER H134
- K974061 — RECHARGEABLE BATTERY PART NUMBER GL825-200
- K973851 — ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY #M12/630
Adverse events under product code MOQ
product code MOQ- Malfunction
- 1,643
- Total
- 1,643
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.