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510(k) K914077

REPEL(TM) LITE CUT RESISTANT GLOVE LINERS by Depuy-Raynham — Product Code LYU

K914077 is an FDA 510(k) premarket notification submitted by Depuy-Raynham for the device "REPEL(TM) LITE CUT RESISTANT GLOVE LINERS". The FDA issued a decision of Substantially Equivalent on December 2, 1991. The device falls under product code LYU (Accessory, Surgical Apparel), a Class I device regulated under 21 CFR 878.4040. Depuy-Raynham has at least 2 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 2, 1991
Date Received
September 11, 1991
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Accessory, Surgical Apparel
Device Class
Class I
Regulation Number
878.4040
Review Panel
HO
Submission Type

Other clearances by Depuy-Raynham

  • K910941 — LIFELINER SURGICAL GLOVE (May 9, 1991)
  • K900310 — REPEL SURGICAL GLOVE LINERS (March 1, 1990)

Other clearances for product code LYU

  • K011755 — STRYKER T4 HYTREL (R) TOGAS (June 22, 2001)
  • K965237 — NURSES BOUFFANT CAP (August 27, 1997)
  • K970988 — FAR-EAST BOUFFANT CAPS (July 10, 1997)
  • K964364 — DISPOSABLE APRON (February 25, 1997)
  • K961791 — DEPUY DISPOSABLE FILTER/HOOD (August 9, 1996)
  • K961454 — AMMI MAGNI-GUARD (July 25, 1996)
  • K945302 — SLOAN STA-DRI PANT PROTECTOR (March 19, 1996)
  • K954314 — ULTRAFIT LINERS (December 28, 1995)
  • K953089 — I-SPOUSE (October 16, 1995)
  • K952303 — SPLASH ASSIST (August 24, 1995)

FDA data resources