Conphar Deluxe Aneroid Sphygmomanometer

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K801186 ↗

FDA Product Code

DXQ

Device Class

Class II

Regulation

21 CFR Part 870.1120

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

• Mayo Scissor Curyed 5 1/2

  Class I

  FDA 510(k) K821276 Active Cleared 28 May 1982

• Crile, Curved Forceps 5 1/2

  Class I

  FDA 510(k) K821281 Active Cleared 27 May 1982

• Mayo-Hegar Needle Holder

  Class I

  FDA 510(k) K821289 Active Cleared 3 Jun 1982

• Backhaus Clamp, 5 1/4

  Class I

  FDA 510(k) K821293 Active Cleared 28 May 1982

• Kelly Forceps Curved 5 1/2

  Class I

  FDA 510(k) K821277 Active Cleared 27 May 1982

• Crile Forceps Straight 5 1/2

  Class I

  FDA 510(k) K821287 Active Cleared 27 May 1982

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