Atlas FDA

COMPRESSION LEGGING DEVICE

FDA 510(k) clearance K871889 · decided 1987-08-04

Clearance details

K-number
K871889
Device name
COMPRESSION LEGGING DEVICE
Applicant
A-T Surgical Mfg. Co., Inc.
Decision
Substantially Equivalent
Date received
1987-05-15
Decision date
1987-08-04
Days to decision
81 days
Clearance type
Traditional
Product code
LLK
Device class
2
Regulation number
880.5780
Medical specialty
General Hospital
Advisory committee
General Hospital
Location
Holyoke, 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
UNNA-SLEEVE(TM) (K903532)Aci Medical, Inc.1990-11-02
TECNOL COMPRESSION KNEE DRESSING (K873368)Tecnol New Jersey Wound Care, Inc.1987-12-11
MODEL 1888 ALPHA COS/RESPIRATION CAR (K834460)Spacelabs, Inc.1984-02-13

Recalls involving this device

No recalls on record reference this clearance.