Atlas FDA

DMI SERIES 90 EXAMINATION TABLE

FDA 510(k) clearance K894788 · decided 1989-09-08

Clearance details

K-number
K894788
Device name
DMI SERIES 90 EXAMINATION TABLE
Applicant
M.D. Intl., Inc.
Decision
Substantially Equivalent
Date received
1989-07-28
Decision date
1989-09-08
Days to decision
42 days
Clearance type
Traditional
Product code
KMN
Device class
1
Regulation number
880.6140
Medical specialty
General Hospital
Advisory committee
General Hospital
Location
Salt Lake City, UT, 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
PAD, EXAMINING TABLE (K801936)Volunteer Blind Industries, Inc.1980-08-27
BED TRAY (K761110)Fred Sammons, Inc.1976-12-02

Recalls involving this device

No recalls on record reference this clearance.