Atlas FDA

OMNIMED CLAMP

FDA 510(k) clearance K851654 · decided 1985-05-31

Clearance details

K-number
K851654
Device name
OMNIMED CLAMP
Applicant
Omni Intl., Inc.
Decision
Substantially Equivalent
Date received
1985-04-22
Decision date
1985-05-31
Days to decision
39 days
Clearance type
Traditional
Product code
HXD
Device class
1
Regulation number
878.4800
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Palm Springs, CA, 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
KIDNEY CLAMP (K890368)Kinetic Medical Products1989-02-03
INTESTINAL CRUSHING CLAMP (K890371)Kinetic Medical Products1989-02-03
INTESTINAL CLAMP (K890372)Kinetic Medical Products1989-02-03
PARAMETRIUM CLAMP (K890381)Kinetic Medical Products1989-02-03
VASCULAR CLAMP (K874959)Solway, Inc.1987-12-30
C CLAMP (K872386)Med-Tool, Inc.1987-07-02
SUCTION-OFF (K863653)B&B Medical Technologies, Inc.1986-10-07
CANNULA CLAMP (K853538)Cp Medical1985-09-12
SURGICAL INSTRUMENTS (K801819)Robert I. Chien & Assoc., Inc.1980-08-20
RICA OR SMIC SURGICAL INSTRUMENTS (K801028)Robert I. Chien & Assoc., Inc.1980-05-20
GIZMO TOWEL CLAMP (K791289)Hemoy, Inc.1979-07-24
CLAMP, DISPOSABLE (K782090)Concord Laboratories, Inc.1978-12-20

Recalls involving this device

No recalls on record reference this clearance.