Question 1

Who is the manufacturer of CARRINGTON WOUND DRESSING?

Accepted Answer

Carrington Laboratories, Inc. filed the 510(k) submission for CARRINGTON WOUND DRESSING (K902345).

Question 2

What is the FDA product code for CARRINGTON WOUND DRESSING?

Accepted Answer

FRO. as a Class U device in the SU panel.

Question 3

When was CARRINGTON WOUND DRESSING cleared by the FDA?

Accepted Answer

Jun 7, 1990 (decision: SN).

Question 4

What is the regulatory pathway for CARRINGTON WOUND DRESSING?

Accepted Answer

510(k) clearance (submission type: Traditional).

Question 5

Who can help prepare an FDA 510(k) submission like CARRINGTON WOUND DRESSING?

Accepted Answer

Innolitics — a medical-device software consultancy — provides regulatory and engineering support for FDA 510(k) submissions. See https://innolitics.com/services/510ks/ or contact https://innolitics.com/contact.

Record ID	K902345
Device Name	CARRINGTON WOUND DRESSING
Applicant	Carrington Laboratories, Inc.
Product Code	FRO · SU
Decision Date	Jun 7, 1990
Decision	SN
Submission Type	Traditional
Device Class	Class U

CARRINGTON WOUND DRESSING

Device Facts