Maxicamera Model 200A
FDA 510(k) K827543 · General Electric Co.
510(k) numberK827543
Submission
- Device name
- Maxicamera Model 200A
- Applicant
- General Electric Co.
Des Plaines, IL, US - Received
- May 25, 1982
- Decision date
- July 9, 1982
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
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Questions and answers
When was Maxicamera Model 200A cleared by the FDA?
Maxicamera Model 200A (K827543) received a 510(k) decision of Substantially Equivalent on July 9, 1982, 45 days after the submission was received.