FDA 510(k)

MEDI-JECT

K-Number: K832847 · 1984-02-28

Decision Date1984-02-28

Product CodeKZH

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

MEDI-JECT is the device name listed in this FDA 510(k) record. The listed applicant is Jack H. Ritterskamp. It received FDA 510(k) clearance on 1984-02-28 under 510(k) number K832847. The device is classified under product code KZH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDI-JECT?

MEDI-JECT is a medical device that received FDA 510(k) clearance on 1984-02-28. The listed applicant is Jack H. Ritterskamp. The 510(k) number is K832847.

When did MEDI-JECT receive FDA 510(k) clearance?

MEDI-JECT received FDA 510(k) clearance on 1984-02-28, under 510(k) number K832847.

Who is the listed applicant for MEDI-JECT?

The FDA 510(k) record lists Jack H. Ritterskamp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDI-JECT?

The FDA product code for MEDI-JECT is KZH.

Related Devices (Code: KZH)

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.

K243232GripMateSynthon Hispania S.L.K213429AccuSert Needle InserterEmed Technologies Corporation K163400Orbit InserterYpsomed AG K160860MiniMed Quick-serterMedtronic Minimed K124026LOBSTER AUTO-INJECTORScandinavian Health Limited K122837AUTOJECT 2 FOR GLASSY SYRINGEOwen Mumford, Ltd.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.