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510(k) K827816

PODIATRY X-RAY UNIT by The S. S. White Co.

K827816 is an FDA 510(k) premarket notification submitted by The S. S. White Co. for the device "PODIATRY X-RAY UNIT". The FDA issued a decision of Substantially Equivalent on August 24, 1982. The S. S. White Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 24, 1982
Date Received
July 26, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by The S. S. White Co.

  • K852745 — PORCELAIN VENEER SYSTEM BONDING KIT (August 16, 1985)
  • K852744 — CHARACTERIZER KIT VISIBLE LIGHT CURED RESTOR-COLOR (August 16, 1985)
  • K853005 — S.S. WHITE DENTAL X-RAY FILM HOLDER & ALIGNING ARM (August 13, 1985)
  • K852743 — PORCELAIN VENEER SYSTEM LABORATORY KIT (July 31, 1985)
  • K852182 — EASY TRAY & EASY BASE CUSTOM IMPRESSION TRAY MATER (July 2, 1985)
  • K837440 — UNKNOWN (June 10, 1983)
  • K781293 — RESTORATIVE SYSTEM PROFILE (August 18, 1978)
  • K771938 — ALGINATE IMPRESSION MATERIAL (November 2, 1977)
  • K770093 — DENTAL BURS (January 24, 1977)
  • K760369 — POWDERLITE (August 11, 1976)

FDA data resources