Atlas FDA

SUBOCCIPITAL ICE PILLOW

FDA 510(k) clearance K882413 · decided 1988-11-30

Clearance details

K-number
K882413
Device name
SUBOCCIPITAL ICE PILLOW
Applicant
Ferguson Medical
Decision
Substantially Equivalent
Date received
1988-06-13
Decision date
1988-11-30
Days to decision
170 days
Clearance type
Traditional
Product code
IME
Device class
1
Regulation number
890.5700
Medical specialty
Physical Medicine
Advisory committee
Physical Medicine
Location
Chico, 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
COLD PACK (K923627)Friendmed Products1993-04-14
HOTPAD (K915876)Ten Comfort Corp.1993-02-12
HOT OR COLD PACK (THERMIPAQ) (K921446)Thermionics Corp.1992-07-13
MICRO-AIRE SOFT-ICE, COLD THERAPY COMPRESS (K905207)Micro Surgical Instruments Corp.1991-01-22
RE-HEATER, HOT PACK (K863654)K & L Ent.1986-10-23
NICE PACK (K832193)Universal Medical Instrument Corp.1983-08-31
ENSWELL (K831899)Dr. Micheal A. Sabia1983-07-07
MICROPAK MOIST HEAT PAD (K830981)Micropak Manufacturers, Inc.1983-06-03
ICY COLD ICE CAP (K830416)Ladora Ent.1983-03-10
THERMOELASTOMER HOT/COLD COMPRESS BK7186 (K823649)Fred Sammons, Inc.1983-01-21
THERMOELASTOMER HOT/COLD COMPRESS-7187- (K823650)Fred Sammons, Inc.1983-01-21
HOT/COLD PACK HOLDERS (K823814)Danek Medical, Inc.1983-01-14

Recalls involving this device

No recalls on record reference this clearance.