Atlas FDA

MODEL 2001 PHACOEMULSIFIER ASPIRATOR

FDA 510(k) clearance K880968 · decided 1988-04-19

Clearance details

K-number
K880968
Device name
MODEL 2001 PHACOEMULSIFIER ASPIRATOR
Applicant
Mcghan Instrumed Corp.
Decision
Substantially Equivalent
Date received
1988-03-08
Decision date
1988-04-19
Days to decision
42 days
Clearance type
Traditional
Product code
HQE
Device class
2
Regulation number
886.4150
Medical specialty
Ophthalmic
Advisory committee
Ophthalmic
Location
Salt Lake City, UT, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.