Medical Device Manufacturer · US , Williamsburg , VA

Spectra Medical Devices, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2008

6

Total

6

Cleared

0

Denied

Spectra Medical Devices, Inc. has 6 FDA 510(k) cleared medical devices. Based in Williamsburg, US.

Historical record: 6 cleared submissions from 2008 to 2016. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Spectra Medical Devices, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Spectra Medical Devices, Inc.

6 devices

1-6 of 6

Cleared Feb 05, 2016

SPECTRA Disposable Single Lumen Echogenic Injection Anesthesia Conduction Needle

Anesthesiology · 290d

Cleared Jul 29, 2011

SODIUM CHLORIDE INJECTION, 0.9%, USP 5 ML, 10 ML AMPULE

General Hospital · 219d

Cleared Mar 20, 2009

STERILE SODIUM CHLORIDE 0.9% FLUSH, 5ML, 10ML, AMPULE

General Hospital · 186d

Cleared Dec 08, 2008

SPECTRA GUIDEWIRE INTRODUCER NEEDLE

Cardiovascular · 94d

Cleared Nov 28, 2008

SPECTRA-GLASS LOR (LOSS OF RESISTANCE SYRINGE, 5CC METAL L/S OR L/L TIP,...

General Hospital · 74d

Cleared Jul 29, 2008

SPECTRA-LOR, 10 ML PLASTIC LOSS OF RESISTANCE SYRINGE, L/S, SPECTRA-LOR, 10ML...

General Hospital · 57d