K827577Substantially Equivalent
Variable Contrast Acuiometer, Diagnostic Laser Interferometer
Randwal Instrument Co., Inc., Southbridge MA / Traditional, Substantially Equivalent
K827577 is the FDA 510(k) clearance record for VARIABLE CONTRAST ACUIOMETER, DIAGNOSTIC LASER INTERFEROMETER, cleared for Randwal Instrument Co., Inc. on . FDA records list 6 510(k) clearances for Randwal Instrument Co., Inc., from to . As of , FDA records show no recalls naming K827577.
Clearance record
- Decision date
- Received
- (35 days to decision)
- Review panel
- Unknown
- Applicant
- Randwal Instrument Co., Inc. P.O.Box A, 100 Mechanic St., Southbridge MA
- Third party review
- No
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