Atlas FDA

ARGYLE DELEE SUCTION CATHETER W/MUCOUS

FDA 510(k) clearance K820572 · decided 1982-04-09

Clearance details

K-number
K820572
Device name
ARGYLE DELEE SUCTION CATHETER W/MUCOUS
Applicant
Sherwood Medical Co.
Decision
Substantially Equivalent
Date received
1982-03-02
Decision date
1982-04-09
Days to decision
38 days
Clearance type
Traditional
Product code
KTR
Device class
2
Regulation number
874.4680
Medical specialty
Ear, Nose, Throat
Advisory committee
Ear, Nose, Throat
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
BAL CATH (K923487)Ballard Medical Products1993-07-30
RIGID SUCTION TIPS (K822255)Kelleher Corp.1982-08-25
ARGYLE TAUSSIG CULTURE CATHETER (K791327)Sherwood Medical Co.1979-08-22

Recalls involving this device

No recalls on record reference this clearance.