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510(k) K801310

THE MAGTEC SYSTEM by Valley Forge Scientific Corp.

K801310 is an FDA 510(k) premarket notification submitted by Valley Forge Scientific Corp. for the device "THE MAGTEC SYSTEM". The FDA issued a decision of Substantially Equivalent on Jun 20, 1980. Valley Forge Scientific Corp. has 26 other 510(k) clearances on record.

Clearance details

Decision
SESE (Substantially Equivalent)
Decision Date
Jun 20, 1980
Date Received
Jun 3, 1980
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Valley Forge Scientific Corp.

  • K050364 — MALIS 2000 BIPOLAR ELECTROSURGICAL SYSTEM (Mar 9, 2005)
  • K042604 — VALLY FORGE SCIENTIFIC MALIS BIPOLAR DISPOSABLE FINGER OPERATED ELECTROSURGICAL… (Oct 22, 2004)
  • K032601 — STRYKER INTERVENTIONAL PAIN RF GENERATOR (Apr 1, 2004)
  • K033499 — MALIS IRRIGATION MODULE 1000 (Nov 28, 2003)
  • K982229 — BI-DENT (Aug 13, 1998)
  • K973554 — VALLEY FORGE BIPOLAR BALL TIP ELECTRODE (Dec 19, 1997)
  • K971986 — VALLEY FORGE BIPOLAR LOOP (Aug 26, 1997)
  • K964143 — MINI-SYMM BIPOLAR COAGULATOR (Jan 9, 1997)
  • K955764 — VALLEY FORGE BIPLOAR LOOP (Mar 1, 1996)
  • K955346 — VFS - 300 BIPOLAR ELECTROSURGERY SYSTEM (Dec 8, 1995)

FDA data resources

Source: FDA 510(k) database entry for K801310. Report a data issue: hello@regdatalab.com.