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)

HENKE JECT PRESSURE SYRINGE

K-Number: K830524 · 1983-03-24

Decision Date1983-03-24
Product CodeEJI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

HENKE JECT PRESSURE SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Smith & Nephew, Mpl Division. It received FDA 510(k) clearance on 1983-03-24 under 510(k) number K830524. The device is classified under product code EJI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HENKE JECT PRESSURE SYRINGE?

HENKE JECT PRESSURE SYRINGE is a medical device that received FDA 510(k) clearance on 1983-03-24. The listed applicant is Smith & Nephew, Mpl Division. The 510(k) number is K830524.

When did HENKE JECT PRESSURE SYRINGE receive FDA 510(k) clearance?

HENKE JECT PRESSURE SYRINGE received FDA 510(k) clearance on 1983-03-24, under 510(k) number K830524.

Who is the listed applicant for HENKE JECT PRESSURE SYRINGE?

The FDA 510(k) record lists Smith & Nephew, Mpl Division as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HENKE JECT PRESSURE SYRINGE?

The FDA product code for HENKE JECT PRESSURE SYRINGE is EJI.

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 Smith & Nephew, Mpl Division 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 9 devices →

Related Devices (Code: EJI)

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.

↑