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510(k) K802060

STERILE TONSIL SPONGES by Medspec Corp. — Product Code GDY

K802060 is an FDA 510(k) premarket notification submitted by Medspec Corp. for the device "STERILE TONSIL SPONGES". The FDA issued a decision of Substantially Equivalent on October 10, 1980. The device falls under product code GDY (Gauze/Sponge, Internal, X-Ray Detectable), a Class I device regulated under 21 CFR 878.4450. Medspec Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 10, 1980
Date Received
August 25, 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 Medspec Corp.

  • K813012 — STERILE BASIN SETS (November 6, 1981)
  • K812711 — STERILE GAUZE PADS 12PLY (November 2, 1981)
  • K812707 — STERILE DISSECTOR SPONGES-X-RAY DETECT (November 2, 1981)
  • K812710 — STERILE LAPAROTOMY SPONGES-X-RAY DETECT (November 2, 1981)
  • K812709 — STERILE DENTAL ROLL (October 23, 1981)
  • K810071 — STERILE SILICONE TUBING (February 12, 1981)
  • K810069 — STERILE AIRWAY (February 2, 1981)
  • K801068 — STERILE ABDOMINAL PAD (May 20, 1980)
  • K801069 — STERILE ISOLATION GOWN (May 20, 1980)
  • K800279 — MEDSPEC RUBBER BANDS (May 2, 1980)

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