Skip to content

Fetalscreen

by Ortho Diagnostic Systems, Inc. 510(k)

Active United States

510(k) K820199

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK820199 Date12 May 1982ClearedStatusActive

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 11 Oct 2026.

Specification

510(k)

510(k) Number
Advisory Committee
Unknown
FDA Decision
SESE Substantially Equivalent

Other devices from Ortho Diagnostic Systems, Inc.

See all devices from Ortho Diagnostic Systems, Inc. →