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)

HANKS BALANCED SALT MIXTURE H6136

K-Number: K832839 · 1983-09-26

Decision Date1983-09-26
Product CodeKIT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

HANKS BALANCED SALT MIXTURE H6136 is the device name listed in this FDA 510(k) record. The listed applicant is Sigma Chemical Co.. It received FDA 510(k) clearance on 1983-09-26 under 510(k) number K832839. The device is classified under product code KIT. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HANKS BALANCED SALT MIXTURE H6136?

HANKS BALANCED SALT MIXTURE H6136 is a medical device that received FDA 510(k) clearance on 1983-09-26. The listed applicant is Sigma Chemical Co.. The 510(k) number is K832839.

When did HANKS BALANCED SALT MIXTURE H6136 receive FDA 510(k) clearance?

HANKS BALANCED SALT MIXTURE H6136 received FDA 510(k) clearance on 1983-09-26, under 510(k) number K832839.

Who is the listed applicant for HANKS BALANCED SALT MIXTURE H6136?

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

What is the FDA product code for HANKS BALANCED SALT MIXTURE H6136?

The FDA product code for HANKS BALANCED SALT MIXTURE H6136 is KIT.

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 Sigma Chemical Co. 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 231 devices →

Related Devices (Code: KIT)

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.

↑