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)

SUCTION PROBE

K-Number: K803206 · 1981-01-21

Decision Date1981-01-21
Product CodeJOL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SUCTION PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Bemis Health Care. It received FDA 510(k) clearance on 1981-01-21 under 510(k) number K803206. The device is classified under product code JOL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUCTION PROBE?

SUCTION PROBE is a medical device that received FDA 510(k) clearance on 1981-01-21. The listed applicant is Bemis Health Care. The 510(k) number is K803206.

When did SUCTION PROBE receive FDA 510(k) clearance?

SUCTION PROBE received FDA 510(k) clearance on 1981-01-21, under 510(k) number K803206.

Who is the listed applicant for SUCTION PROBE?

The FDA 510(k) record lists Bemis Health Care as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUCTION PROBE?

The FDA product code for SUCTION PROBE is JOL.

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 Bemis Health Care 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 12 devices →

Related Devices (Code: JOL)

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.

↑