Atlas FDA

MODEL 6500 MERCURY ARC LIGHT SOURCE

FDA 510(k) clearance K896008 · decided 1989-12-27

Clearance details

K-number
K896008
Device name
MODEL 6500 MERCURY ARC LIGHT SOURCE
Applicant
Medical Dynamics, Inc.
Decision
Substantially Equivalent
Date received
1989-10-13
Decision date
1989-12-27
Days to decision
75 days
Clearance type
Traditional
Product code
GCP
Device class
2
Regulation number
876.1500
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
Englewood, CO, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
EOS BRAND DISPOSABLE PROCTOSCOPE (K954614)North Eos Industries, Inc.1996-04-10
PORGES UNIVERSAL HANDLES (K896505)Porges Corp.1990-01-30
STEERABLE CATHETER SYSTEM (K862424)Endovations1986-09-22
MOD. ENDOPORT SINGLE-USE TROCAR AND SLEEVE (K860103)Endotherapeutics1986-02-12
MODULAR FIBERSCOPE SYSTEM (K843683)Reichert Scientific Instruments1985-01-18
TAMPONADE BALLOON CUFF (K833859)American Endoscopy, Inc.1984-01-03
ENDOSCOPIC SCLEROTHERAPY BALLOON (K821999)Retech1982-08-27
CCD ENDOSCOPE AND ATTACHMENTS (K801247)Welch Allyn, Inc.1980-07-28
ENDOSCOPE AND ACCESSORIES (K790071)Olympus Corp.1979-04-02
FIBER OPTICS SIGMOIDOSCOPE (K771919)Propper Mfg. Co., Inc.1977-10-20
FIBER OPTICS PROCTOSCOPE (K771920)Propper Mfg. Co., Inc.1977-10-20
FIBEO OPTICS ILLUM. SYSTEM (K771918)Propper Mfg. Co., Inc.1977-10-20

Recalls involving this device

No recalls on record reference this clearance.