Atlas FDA

EXMOOR TYMPANOCENTESIS KIT (TK/1)

FDA 510(k) clearance K973587 · decided 1998-01-23

Clearance details

K-number
K973587
Device name
EXMOOR TYMPANOCENTESIS KIT (TK/1)
Applicant
Exmoor Plastics , Ltd.
Decision
Substantially Equivalent
Date received
1997-09-22
Decision date
1998-01-23
Days to decision
123 days
Clearance type
Traditional
Product code
JZF
Device class
1
Regulation number
874.4420
Medical specialty
Ear, Nose, Throat
Advisory committee
Ear, Nose, Throat
Location
Taunton, GB
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
MIDDLE EAR VIEWER AND FLUID COLLECTOR (K862903)Steven K. Juhn1986-11-24
SHAH SELF-CLEARING MASTOID SUCTION TUBE (K853589)Downs Surgical , Ltd.1985-12-23
MICRO FLUID APPLICATOR (K841357)Treace Medical, Inc.1984-08-24
RIGID SUCTION TIPS & RELATED ITEMS (K822010)Kelleher Corp.1982-08-12

Recalls involving this device

No recalls on record reference this clearance.