Atlas FDA

INTRAOCULAR PRESSURE REDUCER

FDA 510(k) clearance K854873 · decided 1986-02-04

Clearance details

K-number
K854873
Device name
INTRAOCULAR PRESSURE REDUCER
Applicant
Mira, Inc.
Decision
Substantially Equivalent
Date received
1985-12-04
Decision date
1986-02-04
Days to decision
62 days
Clearance type
Traditional
Product code
LCR
Device class
2
Regulation number
862.3900
Medical specialty
Clinical Toxicology
Advisory committee
Clinical Toxicology
Location
Waltham, MA, 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
QMS TOBRAMYCIN (K060998)Seradyn, Inc.2006-07-21
ACS TOBRAMYCIN (K974029)Chiron Diagnostics Corp.1998-02-12
TOBRAMYCIN FLEX REAGENT CARTRIDGE (K962818)Dade Intl., Inc.1996-09-13
BECKMAN ARRAY TOBRAMYCIN (TOB) REAGENT (K952568)Beckman Instruments, Inc.1995-08-08
OPUS(R) TOBRAMYCIN (K911940)Pb Diagnostic Systems, Inc.1991-07-01
VAR AURAL GROM AG/S9,SD8.00.28.5/0.2 NS/S/6823 1.4 (K911613)Exmoor Plastics , Ltd.1991-06-28
DU PONT TOBRAMYCIN ASSAY REAGENTS (K850058)E.I. Dupont DE Nemours & Co., Inc.1985-01-18
IMMPULSE TOBRAMYCIN ASSAY REAGENTS (K840847)Paragon Diagnostics, Inc.1984-04-04
STRATUS TOBRAMYCIN FLUOROMETRIC ENZYM (K832408)American Dade1983-08-26
NEEDLE HOLDERS (K822197)Kelleher Corp.1982-08-16
VIRGO IMMUNO-PRECIPITATION ASSAY TOBRA (K821542)Electro-Nucleonics Laboratories, Inc.1982-06-03
ADVANCE SYSTEM EMIT-AMD TOBRAMYCIN ASSAY (K820130)Syva Co.1982-02-05

Recalls involving this device

No recalls on record reference this clearance.