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510(k) K827069

PODIOSCOPE BY ARROW by Arrow X-Ray Corp.

K827069 is an FDA 510(k) premarket notification submitted by Arrow X-Ray Corp. for the device "PODIOSCOPE BY ARROW". The FDA issued a decision of Substantially Equivalent on February 18, 1982. Arrow X-Ray Corp. has at least 1 other 510(k) clearance on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 18, 1982
Date Received
January 18, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Arrow X-Ray Corp.

  • K820119 — PODIOSCOPE BY ARROW (February 18, 1982)

FDA data resources