Needle, Spinal, Short Term, Reprocessed

NMR · Class II — Moderate Risk (510(k) clearance required) · Anesthesiology · 21 CFR 868.5150

Classification

FDA Product Code: NMR
Device class: Class II — Moderate Risk (510(k) clearance required)
Regulation: 21 CFR 868.5150
Review panel: AN
Medical specialty: Anesthesiology
Submission type: 1
GMP exempt: N
Life sustaining: N
Implant: N
Third-party review: Y

Definition

Reprocessing validation data for this device type must be included in a 510(k) submission. (70 FR 56911, available at https://www.govinfo.gov/content/pkg/FR-2005-09-29/pdf/05-19510.pdf).

Market data

Cleared 510(k) submissions: 0
Registered establishments: 0

Source

Authoritative: FDA Device Classification database
Machine: JSON-LD · Markdown