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510(k) K822203

KNIFE HANDLE by Kelleher Corp. — Product Code KTG

K822203 is an FDA 510(k) premarket notification submitted by Kelleher Corp. for the device "KNIFE HANDLE". The FDA issued a decision of Substantially Equivalent on August 20, 1982. The device falls under product code KTG (Knife, Ent), a Class I device regulated under 21 CFR 874.4420. Kelleher Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 20, 1982
Date Received
July 23, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Knife, Ent
Device Class
Class I
Regulation Number
874.4420
Review Panel
EN
Submission Type

Other clearances by Kelleher Corp.

  • K822618 — EMERGENCY TRACHEOSTOMY INSTRUMENT SET (January 28, 1983)
  • K822268 — NAGASHIMA NS-III ELECTRONYSTAGMOGRAPH (January 28, 1983)
  • K823083 — ELECTROSURGICAL UNIT (December 7, 1982)
  • K822252 — ENT TREATMENT UNITS (November 22, 1982)
  • K823111 — NYSTYMOGRAPH ACCESS (November 22, 1982)
  • K822272 — HEAD MIRRORS W/HEAD LAMPS & HEAD BANDS (November 10, 1982)
  • K822017 — TYMPANOSTOMY TUBES & VARIOUS TYPES (October 27, 1982)
  • K822257 — VARIOUS TYPES OF LIGHT SOURCE HANDLES (October 26, 1982)
  • K822259 — LARYNGEAL SPATULAS (October 22, 1982)
  • K822004 — FACE SHIELDS (October 20, 1982)

Other clearances for product code KTG

  • K822280 — ENT KNIFE HANDLES (August 30, 1982)
  • K822205 — KNIVES, ENT (August 30, 1982)
  • K822279 — LANCETS FOR EAR SURGERY (August 25, 1982)
  • K822187 — TONSIL DISSECTORS (August 24, 1982)

FDA data resources