Atlas FDA

TINY HALOGEN EXAM LIGHT

FDA 510(k) clearance K896962 · decided 1989-12-29

Clearance details

K-number
K896962
Device name
TINY HALOGEN EXAM LIGHT
Applicant
Jedmed Instrument Co.
Decision
Substantially Equivalent
Date received
1989-12-15
Decision date
1989-12-29
Days to decision
14 days
Clearance type
Traditional
Product code
KZF
Device class
1
Regulation number
880.6320
Medical specialty
General Hospital
Advisory committee
General Hospital
Location
St. Louis, MO, 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
NEVOSCOPE (K954943)Nizar A. Mullani1996-03-27
WELCH ALLYN VIDEO EPISCOPE (K952835)Welch Allyn, Inc.1995-09-22
H 5100, H 5200, H 5300 (K945507)Rudolf Riester GmbH & Co. KG1994-12-09
SPLINT, PNEUMATIC, ARM & SPLINT, PNEUMATIC, LEG (K941869)The Lighthouse For the Blind, Inc.1994-08-03
WAVE FLUORESCENT MAGNIFIER (K936088)Burton Medical Products Corp.1994-04-26
MEDDEV MULTARRAY MEDICAL EXAMINING LIGHT MODIFICATION (K940284)Meddev International Corp.1994-02-28
SKYTRON EXAM LIGHT (K933564)Skytron, Div. the Kmw Group, Inc.1994-02-10
CHROMOPHARE (K935832)Berchtold Holding GmbH1994-02-03
AC-POWERED MEDICAL EXAMINATION LIGHT (K934259)Welch Allyn, Inc.1994-01-28
RITTER MODEL 158 AND 159 EXAM LIGHTS (K932719)Midmark Corp.1993-12-02
VITAPEN (K924447)Vitajet Corp.1993-09-27
MEDDEV MULTARRAY (TM) MEDICAL EXAMINATION LIGHT (K931197)Meddev International Corp.1993-09-23

Recalls involving this device

No recalls on record reference this clearance.