PFIZONIC 200 ULTRASOUND SCANNER— 510(k) K802531

Name: FDA 510(k) clearance K802531
Creator: U.S. Food and Drug Administration
Published: 1980-12-18

Substantially Equivalent

Pfizer Medical Systems, Inc.

FDA 510(k) clearance K802531 for PFIZONIC 200 ULTRASOUND SCANNER, Substantially Equivalent on 1980-12-18. Applicant: Pfizer Medical Systems, Inc.. Device class: 2.

Clearance details

Applicant: Pfizer Medical Systems, Inc.
Product code: Code IYO
Device class: Class 2
Regulation: 21 CFR 892.1560
Advisory panel: Radiology
Date received: 1980-10-16
Decision date: 1980-12-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K802529 — PFIZONIC 100 ULTRASOUND SCANNER1980-12-18
K802530 — PFIZONIC 250 ULTRASOUND SCANNER1980-12-18
K802532 — PFIZONIC 300 ULTRASOUND SCANNER1980-12-18

Adverse events under product code IYO

product code IYO

Malfunction: 3,339
Total: 3,339

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.