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)

SCOTTS TAP WATER SUBSTITUTE

K-Number: K842918 · 1984-09-11

ApplicantE K Ind., Inc.
Decision Date1984-09-11
Product CodeJCC
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

SCOTTS TAP WATER SUBSTITUTE is the device name listed in this FDA 510(k) record. The listed applicant is E K Ind., Inc.. It received FDA 510(k) clearance on 1984-09-11 under 510(k) number K842918. The device is classified under product code JCC. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCOTTS TAP WATER SUBSTITUTE?

SCOTTS TAP WATER SUBSTITUTE is a medical device that received FDA 510(k) clearance on 1984-09-11. The listed applicant is E K Ind., Inc.. The 510(k) number is K842918.

When did SCOTTS TAP WATER SUBSTITUTE receive FDA 510(k) clearance?

SCOTTS TAP WATER SUBSTITUTE received FDA 510(k) clearance on 1984-09-11, under 510(k) number K842918.

Who is the listed applicant for SCOTTS TAP WATER SUBSTITUTE?

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

What is the FDA product code for SCOTTS TAP WATER SUBSTITUTE?

The FDA product code for SCOTTS TAP WATER SUBSTITUTE is JCC.

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 E K Ind., 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.

K842931DRABKIN REAGENTK842938ACETIC ACID 1% V/VK842934DECOLORIZING FLUIC, ACID-ALCOHOL 3%K842937ACETIC ACID 2% V/VK842935ACETIC ACID, 5% V/VK842936ACETIC ACID, 3% V/V

View all 50 devices →

Related Devices (Code: JCC)

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.

K842914WRIGHT STAIN BUFFERE K Ind., Inc.K841423SCOTTS TAP WATER SUBSTITUTE 7Reagent Laboratory, Inc.K811791PHOSPHATE BUFFERED SALINE (1X)Dutchland Laboratories, Inc.K811251CITRATE BUFFERBioscientificK792574MOPSO BUFFERElectrophoresis Corp. of AmericaK770508SMAC SYSTEMMid Tech, 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.

↑