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)

AMINOGLYCOSIDE CONTROLS

K-Number: K761156 · 1976-12-09

ApplicantSupelco, Inc.
Decision Date1976-12-09
Product CodeDAS
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

AMINOGLYCOSIDE CONTROLS is the device name listed in this FDA 510(k) record. The listed applicant is Supelco, Inc.. It received FDA 510(k) clearance on 1976-12-09 under 510(k) number K761156. The device is classified under product code DAS. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMINOGLYCOSIDE CONTROLS?

AMINOGLYCOSIDE CONTROLS is a medical device that received FDA 510(k) clearance on 1976-12-09. The listed applicant is Supelco, Inc.. The 510(k) number is K761156.

When did AMINOGLYCOSIDE CONTROLS receive FDA 510(k) clearance?

AMINOGLYCOSIDE CONTROLS received FDA 510(k) clearance on 1976-12-09, under 510(k) number K761156.

Who is the listed applicant for AMINOGLYCOSIDE CONTROLS?

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

What is the FDA product code for AMINOGLYCOSIDE CONTROLS?

The FDA product code for AMINOGLYCOSIDE CONTROLS is DAS.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Supelco, 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.

K894141LIQUID CHROMATOGRAPHY COLUMNSK884403LIQUID CHROMATOGRAPHY COLUMNS SOLID PHASE EX. TUBEK883615LIQUID CHROMATOGRAPHY COLUMNS 5-7070/71/72/73K881868LIQUID CHROMATOGRAPHY COLUMNS HISEP COLUMN & GUARDK881361SOLID PHASE EXTRACTION TUBESK880724LIQUID CHROMATO. COLUMNS

View all 24 devices →

Related Devices (Code: DAS)

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.

K982023PELICALSS HUMAN IGG SUBCLASS NEPHLOMETRIC ARRAY KITInova Diagnostics, Inc.K944876HUMAN IGG SUBCLASSES NEPHELOMETRIC BNA KITResearch Diagnostics, Inc.K943098HUMAN IGG SUBCLASSES ELISA COMBI KITResearch Diagnostics, Inc.K943205HUMAN IGG SUBCLASSES RID COMBI KIT (MODIFICATION)Research Diagnostics, Inc.K895600HUMAN (IGG) SUBCLASS (EIA) KITThe Binding Site, Ltd.K790708ANTISERUM TO HUMAN IG G FC FRAGMENTSKent Laboratories, Inc.

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.

↑