Atlas FDA

PF TEST

FDA 510(k) clearance K884513 · decided 1989-02-03

Clearance details

K-number
K884513
Device name
PF TEST
Applicant
Medi-Tech, Inc.
Decision
Substantially Equivalent
Date received
1988-10-27
Decision date
1989-02-03
Days to decision
99 days
Clearance type
Traditional
Product code
GMZ
Device class
1
Regulation number
866.3255
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Somerset, NJ, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.