Atlas FDA

TECNOL COMPRESSION KNEE DRESSING

FDA 510(k) clearance K873368 · decided 1987-12-11

Clearance details

K-number
K873368
Device name
TECNOL COMPRESSION KNEE DRESSING
Applicant
Tecnol New Jersey Wound Care, Inc.
Decision
Substantially Equivalent
Date received
1987-08-21
Decision date
1987-12-11
Days to decision
112 days
Clearance type
Traditional
Product code
LLK
Device class
2
Regulation number
880.5780
Medical specialty
General Hospital
Advisory committee
General Hospital
Location
Fort Worth, TX, 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
COMPRESSION LEGGING DEVICE (K871889)A-T Surgical Mfg. Co., Inc.1987-08-04
MODEL 1888 ALPHA COS/RESPIRATION CAR (K834460)Spacelabs, Inc.1984-02-13

Recalls involving this device

No recalls on record reference this clearance.