Atlas FDA

DISPOSABLE MICROTOME BLADE

FDA 510(k) clearance K831308 · decided 1983-05-16

Clearance details

K-number
K831308
Device name
DISPOSABLE MICROTOME BLADE
Applicant
Surgipath Medical Industries, Inc.
Decision
Substantially Equivalent
Date received
1983-04-22
Decision date
1983-05-16
Days to decision
24 days
Clearance type
Traditional
Product code
IDL
Device class
1
Regulation number
864.3010
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
KNIFE MAKER (K863616)Surgipath Medical Industries, Inc.1986-09-25
DISPOSABLE MICROTOME BLADES (K831921)Polymer Technology Corp.1983-07-29
TISSUE PROCESSING CASSETTES & ACCESS (K813430)American Optical Corp.1981-12-29
TISSUE-TEK III MICROJECT DISP. BLADE SYS (K801426)Miles Laboratories, Inc.1980-07-28

Recalls involving this device

No recalls on record reference this clearance.