Atlas FDA

F.A. MOUNTING MEDIUM

FDA 510(k) clearance K781388 · decided 1978-08-21

Clearance details

K-number
K781388
Device name
F.A. MOUNTING MEDIUM
Applicant
Flow Laboratories, Inc.
Decision
Substantially Equivalent
Date received
1978-08-10
Decision date
1978-08-21
Days to decision
11 days
Clearance type
Traditional
Product code
KEQ
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
SCOTTS TAP WATER SUBSTITUTE CONCENTRATE (K830515)Surgipath Medical Industries, Inc.1983-03-31
VASPAR SEALANT (K792702)Meridian Diagnostics, Inc.1980-01-24
KOH MOUNTING FLUID W/GLYCEROL (K792709)Meridian Diagnostics, Inc.1980-01-24
LACTO-PHENOL ANALINE BLUE FLUID (K792703)Meridian Diagnostics, Inc.1980-01-24
DROPPER, CEPTI-SEAL LAVTOPHENOL (K781868)Marion Laboratories, Inc.1978-11-22
DROPPER, CEPTI-SEAL KOH SOLUTION (K781869)Marion Laboratories, Inc.1978-11-22

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
3M BRAND MICROBIAL PROFILE SYSTEM (N50538/S001)Flow Laboratories, Inc.1981-04-17
FLOW MIC SYSTEM (N50538)Flow Laboratories, Inc.1980-07-15