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)

MONOJECT CORVAC STAT VAC TUBE W/THROM

K-Number: K820717 · 1982-04-01

Decision Date1982-04-01
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MONOJECT CORVAC STAT VAC TUBE W/THROM is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Co.. It received FDA 510(k) clearance on 1982-04-01 under 510(k) number K820717. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MONOJECT CORVAC STAT VAC TUBE W/THROM?

MONOJECT CORVAC STAT VAC TUBE W/THROM is a medical device that received FDA 510(k) clearance on 1982-04-01. The listed applicant is Sherwood Medical Co.. The 510(k) number is K820717.

When did MONOJECT CORVAC STAT VAC TUBE W/THROM receive FDA 510(k) clearance?

MONOJECT CORVAC STAT VAC TUBE W/THROM received FDA 510(k) clearance on 1982-04-01, under 510(k) number K820717.

Who is the listed applicant for MONOJECT CORVAC STAT VAC TUBE W/THROM?

The FDA 510(k) record lists Sherwood Medical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MONOJECT CORVAC STAT VAC TUBE W/THROM?

The FDA product code for MONOJECT CORVAC STAT VAC TUBE W/THROM is JKA.

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 Sherwood Medical Co. 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 191 devices →

Related Devices (Code: JKA)

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.

↑