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)

8 LATEX EXTENSION TUBE WITH CONNECTOR

K-Number: K761360 · 1977-01-10

Decision Date1977-01-10
Product CodeKNX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

8 LATEX EXTENSION TUBE WITH CONNECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Intermed, Inc.. It received FDA 510(k) clearance on 1977-01-10 under 510(k) number K761360. The device is classified under product code KNX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 8 LATEX EXTENSION TUBE WITH CONNECTOR?

8 LATEX EXTENSION TUBE WITH CONNECTOR is a medical device that received FDA 510(k) clearance on 1977-01-10. The listed applicant is Intermed, Inc.. The 510(k) number is K761360.

When did 8 LATEX EXTENSION TUBE WITH CONNECTOR receive FDA 510(k) clearance?

8 LATEX EXTENSION TUBE WITH CONNECTOR received FDA 510(k) clearance on 1977-01-10, under 510(k) number K761360.

Who is the listed applicant for 8 LATEX EXTENSION TUBE WITH CONNECTOR?

The FDA 510(k) record lists Intermed, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 8 LATEX EXTENSION TUBE WITH CONNECTOR?

The FDA product code for 8 LATEX EXTENSION TUBE WITH CONNECTOR is KNX.

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 Intermed, Inc. 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 16 devices →

Related Devices (Code: KNX)

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.

↑