Atlas FDA

TETRA NATAL-MAT WATER FLOTATION MAT.

FDA 510(k) clearance K802833 · decided 1980-12-10

Clearance details

K-number
K802833
Device name
TETRA NATAL-MAT WATER FLOTATION MAT.
Applicant
Tetra Group U.S.A., Inc.
Decision
Substantially Equivalent
Date received
1980-11-12
Decision date
1980-12-10
Days to decision
28 days
Clearance type
Traditional
Product code
IKY
Device class
1
Regulation number
880.5150
Medical specialty
General Hospital
Advisory committee
General Hospital
Location
Mchenry, IL, 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
SCM-3 AND ACCESSORIES (K914921)Gaymar Industries, Inc.1992-03-12
GEL FLOTATION MATTRESS (K813226)Jefferson Industries, Inc.1981-12-02
BEDDING PADS EGGCREATE PADS (K802781)Leemart Bedding Mfg. Co.1980-12-10
ECONO-FLOAT WATER FLOTATION MATTRESS (K780779)Jefferson Industries, Inc.1978-05-19
NEONATAL FLOTATION SYSTEM (K772062)Medpro, Inc.1977-11-15
MEDPRO FLOTATION SYSTEM (K771824)Medpro, Inc.1977-10-19
DECUBITUS MATTRESS (K760963)Arco Medical Products Co.1976-11-18

Recalls involving this device

No recalls on record reference this clearance.