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FDA 510(k)

SAFE-N-JECT

K-Number: K852304 · 1985-09-20

Decision Date1985-09-20
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SAFE-N-JECT is the device name listed in this FDA 510(k) record. The listed applicant is Gerstner Intl. Trade. It received FDA 510(k) clearance on 1985-09-20 under 510(k) number K852304. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAFE-N-JECT?

SAFE-N-JECT is a medical device that received FDA 510(k) clearance on 1985-09-20. The listed applicant is Gerstner Intl. Trade. The 510(k) number is K852304.

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

SAFE-N-JECT received FDA 510(k) clearance on 1985-09-20, under 510(k) number K852304.

Who is the listed applicant for SAFE-N-JECT?

The FDA 510(k) record lists Gerstner Intl. Trade as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SAFE-N-JECT?

The FDA product code for SAFE-N-JECT is FMF.

Related Devices (Code: FMF)

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

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

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