Who is the manufacturer of HERCON ANTI. TRANS. DRESSING AS A WOUND DRESSING?

Hercon Laboratories Corp. filed the 510(k) submission for HERCON ANTI. TRANS. DRESSING AS A WOUND DRESSING (K870743).

What is the FDA product code for HERCON ANTI. TRANS. DRESSING AS A WOUND DRESSING?

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

What is the regulatory pathway for HERCON ANTI. TRANS. DRESSING AS A WOUND DRESSING?

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

Who can help prepare an FDA 510(k) submission like HERCON ANTI. TRANS. DRESSING AS A WOUND DRESSING?

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.

HERCON ANTI. TRANS. DRESSING AS A WOUND DRESSING

K870743 · Hercon Laboratories Corp. · FRO · Apr 6, 1987 · SU

Device Facts

Record ID	K870743
Device Name	HERCON ANTI. TRANS. DRESSING AS A WOUND DRESSING
Applicant	Hercon Laboratories Corp.
Product Code	FRO · SU
Decision Date	Apr 6, 1987
Decision	SN
Submission Type	Traditional
Device Class	Class U

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