Atlas FDA

CUPPED FORCEPS

FDA 510(k) clearance K833605 · decided 1984-01-03

Clearance details

K-number
K833605
Device name
CUPPED FORCEPS
Applicant
Microtek Medical, Inc.
Decision
Substantially Equivalent
Date received
1983-10-12
Decision date
1984-01-03
Days to decision
83 days
Clearance type
Traditional
Product code
KAE
Device class
1
Regulation number
874.4420
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
LARYNGASCOPES, FORCEPS, MICRO SUCTION TUBE & REFLE (K853708)Downs Surgical , Ltd.1986-02-14
41-250 TO 41-282 VARIOUS NASAL CUTTING FORCEPS (K851795)Artiberia1985-06-11
19-790 TO 19-1042 DRESSING/SPONGE FORCEPS (K851775)Artiberia1985-06-11
41-180 TO 41-246 VARIOUS NASAL FORCEPS (K851794)Artiberia1985-06-11
GOLD ALLIGATOR FORCEPS (K833608)Microtek Medical, Inc.1984-01-11
MCGEE FORCEPS (K833607)Microtek Medical, Inc.1984-01-03
MICRO & MINI-MICRO ALLIGATOR FORCEPS (K822369)Treace Medical, Inc.1982-09-09
OFFICE ECONO-FORCEPS (K822372)Treace Medical, Inc.1982-09-09
YARMO NASAL CARTILAGE SOFTENER (K812895)American V. Mueller1981-11-02
HILDYARD POST NASAL FORCEP (K772377)Edward Weck, Inc.1978-01-17
COTTLE COLUMELLA FORCEP (K772397)Edward Weck, Inc.1978-01-17
ALLIGATOR CUP FORCEPS (K772396)Edward Weck, Inc.1978-01-17

Recalls involving this device

No recalls on record reference this clearance.