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)

EMPTY SOLUTION TRANSFER CONTAINER 1000

K-Number: K843523 · 1984-10-16

Decision Date1984-10-16
Product CodeKPE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

EMPTY SOLUTION TRANSFER CONTAINER 1000 is the device name listed in this FDA 510(k) record. The listed applicant is Polymer Technology Corp.. It received FDA 510(k) clearance on 1984-10-16 under 510(k) number K843523. The device is classified under product code KPE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EMPTY SOLUTION TRANSFER CONTAINER 1000?

EMPTY SOLUTION TRANSFER CONTAINER 1000 is a medical device that received FDA 510(k) clearance on 1984-10-16. The listed applicant is Polymer Technology Corp.. The 510(k) number is K843523.

When did EMPTY SOLUTION TRANSFER CONTAINER 1000 receive FDA 510(k) clearance?

EMPTY SOLUTION TRANSFER CONTAINER 1000 received FDA 510(k) clearance on 1984-10-16, under 510(k) number K843523.

Who is the listed applicant for EMPTY SOLUTION TRANSFER CONTAINER 1000?

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

What is the FDA product code for EMPTY SOLUTION TRANSFER CONTAINER 1000?

The FDA product code for EMPTY SOLUTION TRANSFER CONTAINER 1000 is KPE.

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 Polymer Technology Corp. 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 23 devices →

Related Devices (Code: KPE)

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.

↑