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510(k) K822164

EAR SPECULI by Kelleher Corp. — Product Code EPY

K822164 is an FDA 510(k) premarket notification submitted by Kelleher Corp. for the device "EAR SPECULI". The FDA issued a decision of Substantially Equivalent on August 11, 1982. The device falls under product code EPY (Speculum, Ent), a Class I device regulated under 21 CFR 878.1800. Kelleher Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 11, 1982
Date Received
July 23, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Speculum, Ent
Device Class
Class I
Regulation Number
878.1800
Review Panel
SU
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)
  • K823111 — NYSTYMOGRAPH ACCESS (November 22, 1982)
  • K822252 — ENT TREATMENT UNITS (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 EPY

  • K950086 — PEDIA PALS, INCORPORATED (February 7, 1995)
  • K925754 — ECONOM (October 8, 1993)
  • K853588 — FIBRELIGHT NASAL SPECULA (December 18, 1985)
  • K834189 — JAKOBI SURG. INSTRUMENTS #7 44/47 (March 6, 1984)
  • K822373 — EAR SURGERY SPECULUM (September 9, 1982)
  • K822370 — UNIVERSAL SPECULUM HOLDER (September 9, 1982)
  • K791123 — EAR AND NOSE SPECULA (July 10, 1979)
  • K780723 — OTOSCOPE SPECULA (May 9, 1978)
  • K772385 — THIN-BLADED NASAL SPECULUM (January 17, 1978)
  • K772380 — FARRIOR OVAL SPECULUM (January 17, 1978)

FDA data resources