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510(k) K791221

TEGTMEIER MAMMOMETER by Aztec Medical Products, Inc.

K791221 is an FDA 510(k) premarket notification submitted by Aztec Medical Products, Inc. for the device "TEGTMEIER MAMMOMETER". The FDA issued a decision of SESP on July 3, 1979. Aztec Medical Products, Inc. has at least 4 other 510(k) clearances on record.

Clearance Details

Decision
SESP ()
Decision Date
July 3, 1979
Date Received
July 3, 1979
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Aztec Medical Products, Inc.

  • K801939 — RHYTIDOMETER (September 26, 1980)
  • K801937 — BLEPHAROMETER (September 16, 1980)
  • K801938 — RHINOMETER (September 9, 1980)
  • K792608 — TEGTMEIER MAMMOMETER (January 4, 1980)

FDA data resources