Syringe 500BC Be #7000

No FDA recalls on record, checked 9 Oct 2026.

510(k) Number

K830898 ↗

FDA Product Code

BXW

Device Class

Class I

Regulation

21 CFR Part 868.1870

Advisory Committee

Anesthesiology

FDA Decision

SESE Substantially Equivalent

• Non-Rebreathing 't' (Be 117)

  Class II

  FDA 510(k) K973066 Active Cleared 3 Feb 1998

• Be 410 Endotracheal Tube/Trach Tube, Pilot Repair

  Class II

  FDA 510(k) K884638 Active Cleared 23 Nov 1988

• Sg-066 Oxygen Enrichment Kit

  Class II

  FDA 510(k) K860077 Active Cleared 18 Feb 1986

• Gas Collhctor Be 155(155-2-3, 154-4)

  Class I

  FDA 510(k) K770632 Active Cleared 8 Apr 1977

• Ms-303-Oxygen Regulator Shield

  Class I

  FDA 510(k) K810679 Active Cleared 17 Apr 1981

• Flex Arm Be 122, Clamp 122-27

  Class I

  FDA 510(k) K770631 Active Cleared 23 May 1977

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