Question 1

Who is the manufacturer of DOBBHOFF(R) RETRIEVAL FORCEPS?

Accepted Answer

Biosearch Medical Products, Inc. filed the 510(k) submission for DOBBHOFF(R) RETRIEVAL FORCEPS (K901744).

Question 2

What is the FDA product code for DOBBHOFF(R) RETRIEVAL FORCEPS?

Accepted Answer

KQW. It is classified under 21 CFR 888.1520 as a Class 1 device in the Orthopedic panel.

Question 3

When was DOBBHOFF(R) RETRIEVAL FORCEPS cleared by the FDA?

Accepted Answer

Jul 3, 1990 (decision: SESE).

Question 4

What is the regulatory pathway for DOBBHOFF(R) RETRIEVAL FORCEPS?

Accepted Answer

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

Question 5

Who can help prepare an FDA 510(k) submission like DOBBHOFF(R) RETRIEVAL FORCEPS?

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	K901744
Device Name	DOBBHOFF(R) RETRIEVAL FORCEPS
Applicant	Biosearch Medical Products, Inc.
Product Code	KQW · Orthopedic
Decision Date	Jul 3, 1990
Decision	SESE
Submission Type	Traditional
Regulation	21 CFR 888.1520
Device Class	Class 1

DOBBHOFF(R) RETRIEVAL FORCEPS

Device Facts

Regulatory Classification

Identification