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)

STERILE SALINE SOLUTION

K-Number: K093367 · 2010-09-10

Decision Date2010-09-10
Product CodeLPN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

STERILE SALINE SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Cachet Pharmaceuticals Pvt. , Ltd.. It received FDA 510(k) clearance on 2010-09-10 under 510(k) number K093367. The device is classified under product code LPN. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILE SALINE SOLUTION?

STERILE SALINE SOLUTION is a medical device that received FDA 510(k) clearance on 2010-09-10. The listed applicant is Cachet Pharmaceuticals Pvt. , Ltd.. The 510(k) number is K093367.

When did STERILE SALINE SOLUTION receive FDA 510(k) clearance?

STERILE SALINE SOLUTION received FDA 510(k) clearance on 2010-09-10, under 510(k) number K093367.

Who is the listed applicant for STERILE SALINE SOLUTION?

The FDA 510(k) record lists Cachet Pharmaceuticals Pvt. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STERILE SALINE SOLUTION?

The FDA product code for STERILE SALINE SOLUTION is LPN.

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 Cachet Pharmaceuticals Pvt. , Ltd. 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.

Related Devices (Code: LPN)

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.

↑