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510(k) K841652

OCULAR PRESSURE APPLICATOR by The Lebanon Corp.

K841652 is an FDA 510(k) premarket notification submitted by The Lebanon Corp. for the device "OCULAR PRESSURE APPLICATOR". The FDA issued a decision of Substantially Equivalent on June 1, 1984. The Lebanon Corp. has at least 2 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 1, 1984
Date Received
April 20, 1984
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by The Lebanon Corp.

  • K821689 — LEBANON MICROSCOPE (July 9, 1982)
  • K820526 — RELIEF VALVE-HONAN INTRAOC. PRESSURE (March 25, 1982)

FDA data resources