Maxicamera 400ZS
FDA 510(k) K828544 · General Electric Co.
510(k) numberK828544
Submission
- Device name
- Maxicamera 400ZS
- Applicant
- General Electric Co.
Schenectady, NY, US - Received
- November 18, 1982
- Decision date
- December 20, 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 400ZS cleared by the FDA?
Maxicamera 400ZS (K828544) received a 510(k) decision of Substantially Equivalent on December 20, 1982, 32 days after the submission was received.