Skip to content

Bacticard Strep

by Remel, Inc. 2 variants

510(k) K936021

Bacticard Strep is a Class I device made by Remel, Inc., cleared under FDA 510(k) K936021 on 20 May 1994, active as of 22 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK936021 Date20 May 1994ClearedStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA product code
JTO
FDA applicant
Remel Co.
Device class
Class I
Regulation
21 CFR Part 866.2660
Advisory committee
Microbiology
FDA decision
SESE Substantially Equivalent

Other devices from Remel, Inc.

See all devices from Remel, Inc. →