Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MEDIPART SODA LIME MP-3522

K-Number: K853571 · 1985-10-29

Decision Date1985-10-29
Product CodeCBL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MEDIPART SODA LIME MP-3522 is the device name listed in this FDA 510(k) record. The listed applicant is Medipart Jerry Alexander. It received FDA 510(k) clearance on 1985-10-29 under 510(k) number K853571. The device is classified under product code CBL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDIPART SODA LIME MP-3522?

MEDIPART SODA LIME MP-3522 is a medical device that received FDA 510(k) clearance on 1985-10-29. The listed applicant is Medipart Jerry Alexander. The 510(k) number is K853571.

When did MEDIPART SODA LIME MP-3522 receive FDA 510(k) clearance?

MEDIPART SODA LIME MP-3522 received FDA 510(k) clearance on 1985-10-29, under 510(k) number K853571.

Who is the listed applicant for MEDIPART SODA LIME MP-3522?

The FDA 510(k) record lists Medipart Jerry Alexander as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDIPART SODA LIME MP-3522?

The FDA product code for MEDIPART SODA LIME MP-3522 is CBL.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Medipart Jerry Alexander as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 49 devices →

Related Devices (Code: CBL)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑