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 SOLUTION W/O CA-MG

K-Number: K810766 · 1981-05-08

Decision Date1981-05-08
Product CodeKIP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

HANKS' BALANCED SALT SOLUTION W/O CA-MG is the device name listed in this FDA 510(k) record. The listed applicant is Dutchland Laboratories, Inc.. It received FDA 510(k) clearance on 1981-05-08 under 510(k) number K810766. The device is classified under product code KIP. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HANKS' BALANCED SALT SOLUTION W/O CA-MG?

HANKS' BALANCED SALT SOLUTION W/O CA-MG is a medical device that received FDA 510(k) clearance on 1981-05-08. The listed applicant is Dutchland Laboratories, Inc.. The 510(k) number is K810766.

When did HANKS' BALANCED SALT SOLUTION W/O CA-MG receive FDA 510(k) clearance?

HANKS' BALANCED SALT SOLUTION W/O CA-MG received FDA 510(k) clearance on 1981-05-08, under 510(k) number K810766.

Who is the listed applicant for HANKS' BALANCED SALT SOLUTION W/O CA-MG?

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

What is the FDA product code for HANKS' BALANCED SALT SOLUTION W/O CA-MG?

The FDA product code for HANKS' BALANCED SALT SOLUTION W/O CA-MG is KIP.

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 Dutchland 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.

View all 75 devices →

Related Devices (Code: KIP)

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.

↑