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)

BUFFERED GLYCEROL SALINE

K-Number: K863602 · 1986-09-30

Decision Date1986-09-30
Product CodeJSM
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BUFFERED GLYCEROL SALINE is the device name listed in this FDA 510(k) record. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. It received FDA 510(k) clearance on 1986-09-30 under 510(k) number K863602. The device is classified under product code JSM. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BUFFERED GLYCEROL SALINE?

BUFFERED GLYCEROL SALINE is a medical device that received FDA 510(k) clearance on 1986-09-30. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K863602.

When did BUFFERED GLYCEROL SALINE receive FDA 510(k) clearance?

BUFFERED GLYCEROL SALINE received FDA 510(k) clearance on 1986-09-30, under 510(k) number K863602.

Who is the listed applicant for BUFFERED GLYCEROL SALINE?

The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BUFFERED GLYCEROL SALINE?

The FDA product code for BUFFERED GLYCEROL SALINE is JSM.

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 Bd Becton Dickinson Vacutainer Systems Preanalytic 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 632 devices →

Related Devices (Code: JSM)

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.

↑