OXYGEN SENSORS, MODELS CIR, C2R, R13, R15, RI7MED, R22MED, R23, R24MED, R29MED, T1, T2,T4, T7 & UFO130

Analyzer, Gas, Oxygen, Gaseous-phase

TELEDYNE ANALYTICAL INSTRUMENTS

The following data is part of a premarket notification filed by Teledyne Analytical Instruments with the FDA for Oxygen Sensors, Models Cir, C2r, R13, R15, Ri7med, R22med, R23, R24med, R29med, T1, T2,t4, T7 & Ufo130.

Pre-market Notification Details

• Device ID: K001095
• 510k Number: K001095
• Device Name: OXYGEN SENSORS, MODELS CIR, C2R, R13, R15, RI7MED, R22MED, R23, R24MED, R29MED, T1, T2,T4, T7 & UFO130
• Classification: Analyzer, Gas, Oxygen, Gaseous-phase
• Applicant: TELEDYNE ANALYTICAL INSTRUMENTS 16830 CHESTNUT ST. City Of Industry, CA 91749
• Contact: Ray Khajavi
• Correspondent: Ray Khajavi; TELEDYNE ANALYTICAL INSTRUMENTS 16830 CHESTNUT ST. City Of Industry, CA 91749
• Product Code: CCL
• CFR Regulation Number: 868.1720 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2000-04-04
• Decision Date: 2000-06-30

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
00852470008112	K001095	000
00852470008174	K001095	000
00852470008129	K001095	000
00852470008136	K001095	000
00852470008143	K001095	000
00852470008006	K001095	000
00852470008037	K001095	000
00852470008044	K001095	000
00852470008051	K001095	000
00852470008068	K001095	000
00852470008075	K001095	000
00852470008082	K001095	000
00852470008099	K001095	000
00852470008105	K001095	000
00852470008150	K001095	000