K827543Substantially Equivalent
Maxicamera Model 200A
General Electric Co., Des Plaines IL / Traditional, Substantially Equivalent
K827543 is the FDA 510(k) clearance record for MAXICAMERA MODEL 200A, cleared for General Electric Co. on . FDA records list 256 510(k) clearances for General Electric Co., from to . As of , FDA records show no recalls naming K827543.
Clearance record
- Decision date
- Received
- (45 days to decision)
- Review panel
- Unknown
- Applicant
- General Electric Co. 515 E. Touhy Ave., Des Plaines IL
- Third party review
- No
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