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510(k) K770173

STOCKINETTE by Chase Mfg. Co. — Product Code ILG

K770173 is an FDA 510(k) premarket notification submitted by Chase Mfg. Co. for the device "STOCKINETTE". The FDA issued a decision of Substantially Equivalent on February 8, 1977. The device falls under product code ILG (Stocking, Elastic), a Class I device regulated under 21 CFR 890.3475. Chase Mfg. Co. has at least 9 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 8, 1977
Date Received
January 26, 1977
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Stocking, Elastic
Device Class
Class I
Regulation Number
890.3475
Review Panel
PM
Submission Type

Other clearances by Chase Mfg. Co.

  • K791513 — ADAMCO DUST COVER (October 11, 1979)
  • K790993 — INSTANT HOT & COLD PACKS (September 7, 1979)
  • K790644 — SUBMAX (April 26, 1979)
  • K780033 — MATTRESSES, CONDUCTIVE & COVERS (February 21, 1978)
  • K771792 — ENEMA SET (October 20, 1977)
  • K771791 — NEEDLE COUNTING (October 4, 1977)
  • K770899 — FRACTURE CAST BRACE, POLY (July 21, 1977)
  • K770898 — FRACTURE CAST BRACE KIT, PLASTIC (July 21, 1977)
  • K770900 — CAST BRWM, FRACTURE (July 21, 1977)

Other clearances for product code ILG

  • K833437 — ORTHOPEDIC STOCKINETTE (November 3, 1983)
  • K831540 — COMPRESSOGRIP ELASTIC STUMP SHRINKER# (June 8, 1983)
  • K780612 — STOCKINETTE, STERILE (April 19, 1978)
  • K780547 — STERILE ORTHOPEDIC STOCKINETTE (April 10, 1978)
  • K770346 — ORTHOPEDIC STOCKINETTE (March 7, 1977)
  • K760817 — ORTHOPEDIC TUBULAR STOCKINETTE (October 20, 1976)
  • K760576 — TOURNIWRAP BANDAGE (October 5, 1976)

FDA data resources