GRIP, HOSPITAL UTILITY— 510(k) K781800

Substantially Equivalent

Baka Manufacturing Co., Inc.

FDA 510(k) clearance K781800 for GRIP, HOSPITAL UTILITY, Substantially Equivalent on 1978-12-07. Applicant: Baka Manufacturing Co., Inc..

Clearance details

Applicant: Baka Manufacturing Co., Inc.
Product code: Code KMK
Advisory panel: General Hospital
Date received: 1978-10-23
Decision date: 1978-12-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code KMK

product code KMK

Malfunction: 461
Other: 1
Total: 462

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.