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510(k) K760070

TUMBLER, PERSONAL, ROUND, 9 OUNCE by Bemis Health Care

K760070 is an FDA 510(k) premarket notification submitted by Bemis Health Care for the device "TUMBLER, PERSONAL, ROUND, 9 OUNCE". The FDA issued a decision of Substantially Equivalent on July 20, 1976. Bemis Health Care has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 20, 1976
Date Received
June 18, 1976
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Bemis Health Care

  • K885019 — BEMIS STERILE-CASE FOR USE W/ETHYLENE OXIDE STERI. (January 25, 1989)
  • K822556 — CRITICAL MEASUREMENT UNIT (October 18, 1982)
  • K822557 — SPECIMEN ADAPTOR (October 18, 1982)
  • K803206 — SUCTION PROBE (January 21, 1981)
  • K771737 — SUCTION CANISTER (December 20, 1977)
  • K771733 — 8 EMESIS BASIN (September 28, 1977)
  • K771738 — MALE URINAL (September 28, 1977)
  • K760393 — BED PAN, STACKABLE (AUTOCLAVABLE) (August 23, 1976)
  • K760071 — TRAY, PERSONAL, RECTANG. 8 1/2 X 5 1/4 (July 20, 1976)
  • K760072 — CARAFE, PERSONAL, 1-QT SEMI-RECTANGULAR (July 20, 1976)

FDA data resources