RecallHawk

8X-10-6XXX Camera Head

Santa Barbara Imaging Systems

Summary

Santa Barbara Imaging Systems received 510(k) clearance for 8X-10-6XXX Camera Head, a GCJ device. Cleared on 2023-02-28.

Details

Source

510(k) Clearance

External ID

K223116

Action Date

2023-02-28

Status

Traditional

Category

device

Product Code

GCJ

Product Description

8X-10-6XXX Camera Head. Product code: GCJ.

Context & Analysis

A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 403 device clearances issued this month.

Frequently Asked Questions

What does 510(k) clearance mean?

A 510(k) is an FDA premarket submission demonstrating that a device is substantially equivalent to a legally marketed device. It does NOT mean FDA approval — it means the device is cleared for marketing because it's similar enough to an existing cleared device. Most medical devices reach market via 510(k) rather than full PMA approval.

How often does Santa Barbara Imaging Systems have FDA actions?

This is the only FDA action we have on record for Santa Barbara Imaging Systems in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K223116" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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