Atlas FDA

EMBEDDING RING

FDA 510(k) clearance K831922 · decided 1983-07-29

Clearance details

K-number
K831922
Device name
EMBEDDING RING
Applicant
Polymer Technology Corp.
Decision
Substantially Equivalent
Date received
1983-06-14
Decision date
1983-07-29
Days to decision
45 days
Clearance type
Traditional
Product code
KER
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
MACLEAN-FOGG, DISP. BASE MOLD (K831900)Polymer Technology Corp.1983-07-28
EMBEDDING RINGS (K831333)Surgipath Medical Industries, Inc.1983-05-25
DISPOSABLE BASE MOLD (K831335)Surgipath Medical Industries, Inc.1983-05-16
LANCER BIOPSY HOLDER (K772149)Sherwood Medical Industries1977-11-22

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
BOSTON LENS(R) CLEANER (P820069/S013)Polymer Technology Corp.1994-08-15
THE BOSTON TM CLEANER II (P890054/S001)Polymer Technology Corp.1994-08-15
BOSTON LENS II & IV (P820065/S082)Polymer Technology Corp.1994-02-16
BOSTON LENS II & IV (P820065/S080)Polymer Technology Corp.1993-09-07
BOSTON LENS II & IV (P820065/S081)Polymer Technology Corp.1993-09-07
BOSTON LENS II & IV MANU. & DISTRIBUTOR ADDITION (P820065/S079)Polymer Technology Corp.1992-08-06
BOSTON LENS II & IV MANU. & DISTRIBUTOR ADDITION (P820065/S078)Polymer Technology Corp.1992-04-06
BOSTON LENS II & IV (ITAFOCON A & B) CONTACT LENS (P820065/S077)Polymer Technology Corp.1992-02-20