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510(k) K801768

CONTAIN X-RAY DETECTABLE LAP SPONGE by The Buckeye Cellulose Corp. — Product Code GDY

K801768 is an FDA 510(k) premarket notification submitted by The Buckeye Cellulose Corp. for the device "CONTAIN X-RAY DETECTABLE LAP SPONGE". The FDA issued a decision of Substantially Equivalent on August 20, 1980. The device falls under product code GDY (Gauze/Sponge, Internal, X-Ray Detectable), a Class I device regulated under 21 CFR 878.4450. The Buckeye Cellulose Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 20, 1980
Date Received
July 28, 1980
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Gauze/Sponge, Internal, X-Ray Detectable
Device Class
Class I
Regulation Number
878.4450
Review Panel
SU
Submission Type

Other clearances by The Buckeye Cellulose Corp.

  • K822925 — BOUNDARY SINGLE-USE GOWNS (January 12, 1983)
  • K823173 — ARRIRM SCRUB BRUSH/SPONGE (November 22, 1982)
  • K821564 — BOUNDARY PROCESS CHANGE (July 2, 1982)
  • K820758 — BOUNDARY SINGLE-USE CRANIOTOMY SHEET (April 29, 1982)
  • K820116 — BOUNDARY (February 23, 1982)
  • K813450 — BOUNDARY SINGLE-USE DRAPES (January 22, 1982)
  • K813390 — BONDARY SINGLE-USE OR GOWN (January 5, 1982)
  • K813277 — BOUNDARY DRAPE TAPE (December 18, 1981)
  • K813263 — PATIENT UNDERPAD (November 27, 1981)
  • K812962 — BOUNDARY SURGICAL DRAPE (November 20, 1981)

Other clearances for product code GDY

  • K972634 — ULTRACELL SUCTION SPONGE (December 17, 1997)
  • K960236 — CPR LAP SPONGES (March 28, 1996)
  • K955599 — STRYKER FEMORAL CANAL SPONGE & ACETABULUM SPONGE (February 22, 1996)
  • K955322 — PROTEC X-RAY DETECTABLE GAUZE SPONGE (December 19, 1995)
  • K953830 — KENSORB (October 3, 1995)
  • K953088 — TRIANGULAR SPONGES (September 14, 1995)
  • K953060 — ROSEBUD DISSECTOR (September 14, 1995)
  • K953087 — CHERRY PIT DISSECTOR (September 14, 1995)
  • K953062 — CHERRY DISSECTOR (September 14, 1995)
  • K953059 — KITTNER DISSECTOR (September 14, 1995)

FDA data resources