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510(k) K973554

VALLEY FORGE BIPOLAR BALL TIP ELECTRODE by Valley Forge Scientific Corp. — Product Code JOS

K973554 is an FDA 510(k) premarket notification submitted by Valley Forge Scientific Corp. for the device "VALLEY FORGE BIPOLAR BALL TIP ELECTRODE". The FDA issued a decision of Substantially Equivalent on December 19, 1997. The device falls under product code JOS (Electrode, Electrosurgical), a Class II device regulated under 21 CFR 878.4400. Valley Forge Scientific Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 19, 1997
Date Received
September 19, 1997
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Electrode, Electrosurgical
Device Class
Class II
Regulation Number
878.4400
Review Panel
SU
Submission Type

Other clearances by Valley Forge Scientific Corp.

  • K050364 — MALIS 2000 BIPOLAR ELECTROSURGICAL SYSTEM (March 9, 2005)
  • K042604 — VALLY FORGE SCIENTIFIC MALIS BIPOLAR DISPOSABLE FINGER OPERATED ELECTROSURGICAL (October 22, 2004)
  • K032601 — STRYKER INTERVENTIONAL PAIN RF GENERATOR (April 1, 2004)
  • K033499 — MALIS IRRIGATION MODULE 1000 (November 28, 2003)
  • K982229 — BI-DENT (August 13, 1998)
  • K971986 — VALLEY FORGE BIPOLAR LOOP (August 26, 1997)
  • K964143 — MINI-SYMM BIPOLAR COAGULATOR (January 9, 1997)
  • K955764 — VALLEY FORGE BIPLOAR LOOP (March 1, 1996)
  • K955346 — VFS - 300 BIPOLAR ELECTROSURGERY SYSTEM (December 8, 1995)
  • K951985 — PRECISION BIPOLAR COAGULATOR (May 23, 1995)

Other clearances for product code JOS

  • K161600 — Resection Electrodes (September 6, 2016)
  • K050923 — LIGHTWAVE INTEGRATED ELECTRODE ABLATOR AND LIGHT WAVE INTEGRATED ELECTRODE SUCTI (May 18, 2005)
  • K012684 — REPROCESSED ELECTROSURGICAL ELECTRODE (January 18, 2002)
  • K011515 — MEDLINE GROUNDING PAD (July 13, 2001)
  • K003403 — ENDOSCOPIC MONOPOLAREECTRODE, MODEL EME- 1000 TO 1999 (May 7, 2001)
  • K000333 — STANDARD & EXTENDED BLADE, STANDARD & EXTENDED NEEDLE, STANDARD & EXTENDED BALL, (May 3, 2000)
  • K993885 — ULTRABLATOR ELECTRODE (February 10, 2000)
  • K991830 — CAPSULAR SHRINKAGE ELECTRODE (August 20, 1999)
  • K974735 — STANDARD AND EXTENDED BLADE, NEEDLE AND BALL; MODIFIED STANDARD AND EXTENDED BLA (June 24, 1998)
  • K971187 — STANDARD & EXTENDED BLADE/NEEDLE/BALL;MODIFIED STANDARD & EXTENDED BLADE/NEEDLE (May 5, 1997)

FDA data resources