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CYTOLOGY FIXATIVE

FDA 510(k) clearance K770592 · decided 1977-05-20

Clearance details

K-number
K770592
Device name
CYTOLOGY FIXATIVE
Applicant
Surgipath Medical Industries, Inc.
Decision
Substantially Equivalent
Date received
1977-03-28
Decision date
1977-05-20
Days to decision
53 days
Clearance type
Traditional
Product code
LEA
Device class
1
Regulation number
864.4010
Medical specialty
Pathology
Advisory committee
Pathology
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
TIF FECAL TEST (K873594)Devetec, Inc.1987-09-29
PAP-TRAY II (CATALOG #C600-2) (K761001)Lerner Laboratories, Inc.1976-12-06
PAP-TRAY I (CATALOG #C600-1) (K761000)Lerner Laboratories, Inc.1976-12-06

Recalls involving this device

No recalls on record reference this clearance.