Atlas FDA

OPHTHALMIC CHAIR

FDA 510(k) clearance K844362 · decided 1984-12-11

Clearance details

K-number
K844362
Device name
OPHTHALMIC CHAIR
Applicant
Luneau Laboratories
Decision
Substantially Equivalent
Date received
1984-11-13
Decision date
1984-12-11
Days to decision
28 days
Clearance type
Traditional
Product code
HMF
Device class
1
Regulation number
886.1860
Medical specialty
Ophthalmic
Advisory committee
Ophthalmic
Location
Washington, DC, 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
ROTA SYSTEM 5000 (K935952)Rota Systems Medfurniture, Inc.1994-04-19
ROTA DATAMATE I (K935945)Rota Systems,Inc.1994-04-19
ROTA SYSTEM XL (K931839)Rota Systems Medfurniture, Inc.1993-11-22
MARCO INTERNATIONAL STAND (K930440)Marco Ophthalmic, Inc.1993-07-06
BURTON OPHTHALMIC STAND - MODEL XL3200 (K924771)R.H. Burton Co.1993-04-05
BURTON OPHTHALMIC EXAM UNIT - MODEL 2201 (K924780)R.H. Burton Co.1993-04-05
OPHTHALMIC STAND (K913961)Luneau Ophtalmologie SA1991-12-04
RELIANCE PENDULUM OPHTHALMIC DELIVERY SYSTEM (K853358)Dentsply Intl.1985-10-04
OPHTHALMIC STAND (K844363)Luneau Laboratories1984-12-05
ELECTRIC INSTRUMENT TABLE (K832073)CooperVision, Inc.1983-08-12
RELIANCE OPHTHALMIC INSTRUMENT CONTROL (K812544)F. & F. Koenigkramer1981-09-21
SYSTEM 1 INSTRUMENT STAND (K803195)Surgical Mechanical Research, Inc.1981-02-04

Recalls involving this device

No recalls on record reference this clearance.