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FDA 510(k)

IL VIDEO 22,21 & II ATOMIC SPECTROPHOTO-

K-Number: K830149 · 1983-02-28

ApplicantInstrumentation Laboratory CO
Decision Date1983-02-28
Product CodeDWD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

IL VIDEO 22,21 & II ATOMIC SPECTROPHOTO- is the device name listed in this FDA 510(k) record. The listed applicant is Instrumentation Laboratory CO. It received FDA 510(k) clearance on 1983-02-28 under 510(k) number K830149. The device is classified under product code DWD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IL VIDEO 22,21 & II ATOMIC SPECTROPHOTO-?

IL VIDEO 22,21 & II ATOMIC SPECTROPHOTO- is a medical device that received FDA 510(k) clearance on 1983-02-28. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K830149.

When did IL VIDEO 22,21 & II ATOMIC SPECTROPHOTO- receive FDA 510(k) clearance?

IL VIDEO 22,21 & II ATOMIC SPECTROPHOTO- received FDA 510(k) clearance on 1983-02-28, under 510(k) number K830149.

Who is the listed applicant for IL VIDEO 22,21 & II ATOMIC SPECTROPHOTO-?

The FDA 510(k) record lists Instrumentation Laboratory CO as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IL VIDEO 22,21 & II ATOMIC SPECTROPHOTO-?

The FDA product code for IL VIDEO 22,21 & II ATOMIC SPECTROPHOTO- is DWD.

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Other records listing Instrumentation Laboratory CO 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.

K221359ACL TOP 970 CL, HemosIL CL Anti-Cardiolipin IgM, HemosIL CL Anti-ß2 Glycoprotein-I IgMK223187HemosIL Liquid Anti-XaK223090GEM Premier ChemSTATK223402HemosIL von Willebrand Factor AntigenK213464HemosIL Liquid Anti-XaK213426HemosIL ReadiPlasTin

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Related Devices (Code: DWD)

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.

K992657IBC VRV, MODEL 1350International Biophysics Corp.K920077NIKKISO NK PUMPInternational Medical Products, Inc.K915480B-D ULTRA-VUE PROCEDURE NEEDLE W/ SPINAL TYPE PT.Bd Becton Dickinson Vacutainer Systems PreanalyticK915481B-D ULTRA-VUE PROCEDURE NEEDLE W/ CHIBA TYPE POINTBd Becton Dickinson Vacutainer Systems PreanalyticK915482B-D ULTRA-VUE PROCEDURE NEEDLE W/ WESTCOTT TYPE PTBd Becton Dickinson Vacutainer Systems PreanalyticK905311DURAFLO II HEPARIN TREATED SUCTION WANDS VAR. MOD.Baxter Bentley Laboratories, Inc.

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.

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