Atlas FDA

FORCEPS FOR USE WITH RIGID ENDOSCOPES

FDA 510(k) clearance K822193 · decided 1982-08-24

Clearance details

K-number
K822193
Device name
FORCEPS FOR USE WITH RIGID ENDOSCOPES
Applicant
Kelleher Corp.
Decision
Substantially Equivalent
Date received
1982-07-23
Decision date
1982-08-24
Days to decision
32 days
Clearance type
Traditional
Product code
JEK
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
OPTICAL FORCEPS (K990561)Pilling Weck Surgical1999-05-14
MALLEUS NIPPERS (K822198)Kelleher Corp.1982-08-25

Recalls involving this device

No recalls on record reference this clearance.