Atlas FDA

SPERM-SELECT ADDITIONAL INDICATION

FDA 510(k) clearance K872849 · decided 1987-09-28

Clearance details

K-number
K872849
Device name
SPERM-SELECT ADDITIONAL INDICATION
Applicant
Pharmacia, Inc.
Decision
Substantially Equivalent
Date received
1987-07-20
Decision date
1987-09-28
Days to decision
70 days
Clearance type
Traditional
Product code
HDR
Device class
2
Regulation number
884.5250
Medical specialty
Obstetrics/Gynecology
Advisory committee
Obstetrics/Gynecology
Location
Piscataway, NJ, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
MODELS 011 & 011B IRIDOCAPSULAR IOLS (P810042)Pharmacia, Inc.1982-12-15