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)

TOBRAMYCIN LIQUID CONTROL SERUM

K-Number: K792264 · 1979-12-18

ApplicantHemometrix
Decision Date1979-12-18
Product CodeLAS
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

TOBRAMYCIN LIQUID CONTROL SERUM is the device name listed in this FDA 510(k) record. The listed applicant is Hemometrix. It received FDA 510(k) clearance on 1979-12-18 under 510(k) number K792264. The device is classified under product code LAS. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TOBRAMYCIN LIQUID CONTROL SERUM?

TOBRAMYCIN LIQUID CONTROL SERUM is a medical device that received FDA 510(k) clearance on 1979-12-18. The listed applicant is Hemometrix. The 510(k) number is K792264.

When did TOBRAMYCIN LIQUID CONTROL SERUM receive FDA 510(k) clearance?

TOBRAMYCIN LIQUID CONTROL SERUM received FDA 510(k) clearance on 1979-12-18, under 510(k) number K792264.

Who is the listed applicant for TOBRAMYCIN LIQUID CONTROL SERUM?

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

What is the FDA product code for TOBRAMYCIN LIQUID CONTROL SERUM?

The FDA product code for TOBRAMYCIN LIQUID CONTROL SERUM is LAS.

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 Hemometrix 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 7 devices →

Related Devices (Code: LAS)

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.

↑