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)

COPPER SULFATE SOLUTION SP. GR.1.055

K-Number: K803095 · 1981-03-06

ApplicantAccra Laboratories, Inc.
Decision Date1981-03-06
Product CodeKSL
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

COPPER SULFATE SOLUTION SP. GR.1.055 is the device name listed in this FDA 510(k) record. The listed applicant is Accra Laboratories, Inc.. It received FDA 510(k) clearance on 1981-03-06 under 510(k) number K803095. The device is classified under product code KSL. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COPPER SULFATE SOLUTION SP. GR.1.055?

COPPER SULFATE SOLUTION SP. GR.1.055 is a medical device that received FDA 510(k) clearance on 1981-03-06. The listed applicant is Accra Laboratories, Inc.. The 510(k) number is K803095.

When did COPPER SULFATE SOLUTION SP. GR.1.055 receive FDA 510(k) clearance?

COPPER SULFATE SOLUTION SP. GR.1.055 received FDA 510(k) clearance on 1981-03-06, under 510(k) number K803095.

Who is the listed applicant for COPPER SULFATE SOLUTION SP. GR.1.055?

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

What is the FDA product code for COPPER SULFATE SOLUTION SP. GR.1.055?

The FDA product code for COPPER SULFATE SOLUTION SP. GR.1.055 is KSL.

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 Accra Laboratories, 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.

K851494TWO-STEP ACID FAST BACTERIA STAINK851493KINYOUN ACID FAST STAIN KITK843427GILL PAPANICOLAOU STAIN EA-1 & 2 OG-6K843425HARRIS HEMATOXYLIN, MERCURY FREE, ACIDK843428BIOFIXK843426EOSIN Y 1% ALCOHOLIC

View all 20 devices →

Related Devices (Code: KSL)

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.

K882101HEMOGLOBIN SCREENING DEVICEPortable Medical 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.

↑