STERI-VAC #400C GAS STERILIZER— 510(k) K812867

Clearance details

Applicant

3M Company

Product code

Code FLF

Device class

Class 2

Regulation

21 CFR 880.6860

Advisory panel

General Hospital

Date received

1981-10-13

Decision date

1981-11-02

Decision

Substantially Equivalent

Clearance type

Traditional

Location

Monrovia, CA, US

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Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K812867.