Atlas FDA

SPRIO-LOOP

FDA 510(k) clearance K811419 · decided 1981-06-12

Clearance details

K-number
K811419
Device name
SPRIO-LOOP
Applicant
Datamed, Inc.
Decision
Substantially Equivalent
Date received
1981-05-19
Decision date
1981-06-12
Days to decision
24 days
Clearance type
Traditional
Product code
BTX
Device class
1
Regulation number
878.3910
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Walker, MI, 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
BABY BOARD (K935098)Sentry Medical Products, Inc.1994-02-15
4/1 ARMBOARD (K900175)Infection Control Products, Inc.1990-01-24
ALLEN PRONE ARMBOARD (K884838)Edgewater Medical Systems, Inc.1988-12-15
UNIVERSALLY ADJUSTABLE ARMBOARD (K882524)Karlin Technology, Inc.1988-07-08
ALLEN LATERAL ARMBOARD (K881292)Edgewater Medical Systems, Inc.1988-04-07
BOARD, ARM (WITH COVER) (K864670)Anago, Inc.1987-01-12
ARMBOARD AND THE BOARD (K833664)Rick Robbin & Frederick Auerbach1983-12-27
SAFE-T ARM BOARD (K830018)Harvey A. Turner, M.D.1983-01-26
ARM BOARD W/I.V COVERING (K823412)Sage Products, Inc.1982-12-15
ARM SHIELD FOR ANESTHESIA (K792147)Medical Innovations Corp.1979-12-06
IV ARMBOARDS (K781233)Fibre Formations, Inc.1978-08-14
COVER, ARMBOARD, DISPOSABLE (K770391)Precept, Inc.1977-03-07

Recalls involving this device

No recalls on record reference this clearance.