Atlas FDA

RULER

FDA 510(k) clearance K854892 · decided 1985-12-24

Clearance details

K-number
K854892
Device name
RULER
Applicant
Euro-Med Intl.
Decision
Substantially Equivalent
Date received
1985-12-06
Decision date
1985-12-24
Days to decision
18 days
Clearance type
Traditional
Product code
FTY
Device class
1
Regulation number
878.4800
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Danville, CA, 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
Noxilizer Surgical Ruler (K160501)Noxilizer, Inc.2016-05-26
DISPOSABLE WOUND MEASURE GUIDE, PLASTIC, PROTECTOR, WOUND, PLASTIC (K951064)S-E Sales & Distribution, Inc.1995-05-19
OLYMPIC AUTO-LENGTH (K934930)Olympic Medical Corp.1993-12-29
OLYMPIC INFA-LENGTH (K932112)Olympic Medical Corp.1993-07-22
STRYKER PRESSURE MONITOR SYSTEM (K883485)Stryker Corp.1988-09-13
PEDIATRIC AIRWAY MEASUREMENT SYSTEM & P.A.M.S. (K880441)Plane Iii, Inc.1988-02-18
TUMORIMETER (K874352)Cancer Technologies, Inc.1987-11-23
TEMPLATE (K873470)Cox-Uphuff Intl.1987-09-08
LN 100 BREAST MARKER (K872319)Instrumentation Industries, Inc.1987-08-11
KUNDIN WOUND GAUGE (K863409)Jane I. Kundin1986-09-29
PS2 BRAND FACIAL SYMMETRY GUIDE (LEE DESIGN) (K862576)Professional Services For Surgeons, Ltd.1986-07-15
PS2 BRAND MAMMAPLASTY (K860912)Professional Services For Surgeons, Ltd.1986-03-24

Recalls involving this device

No recalls on record reference this clearance.