FDA applicant

Blood Gas Supply Co.

Melrose, MA1 decision1988–19880 recalls

FDA records 1 decision for Blood Gas Supply Co. (Melrose, MA) in 1988: 1 510(k) clearance. All are in product code DXT (Injector And Syringe, Angiographic). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, cardiovascular panel, where it files most

How often FDA has decided Blood Gas Supply Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Blood Gas Supply Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Blood Gas Supply Co. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Blood Gas Supply Co.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Blood”

FDA records each applicant name separately; these may or may not be the same firm.

Blood Products Specialties, LLC 1

Blood Gas Supply Co.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Blood”