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FDA 510(k)

DOBBHOFF(R) RETRIEVAL FORCEPS

K-Number: K901744 · 1990-07-03

ApplicantBiosearch Medical Products, Inc.
Decision Date1990-07-03
Product CodeKQW
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DOBBHOFF(R) RETRIEVAL FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Biosearch Medical Products, Inc.. It received FDA 510(k) clearance on 1990-07-03 under 510(k) number K901744. The device is classified under product code KQW. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DOBBHOFF(R) RETRIEVAL FORCEPS?

DOBBHOFF(R) RETRIEVAL FORCEPS is a medical device that received FDA 510(k) clearance on 1990-07-03. The listed applicant is Biosearch Medical Products, Inc.. The 510(k) number is K901744.

When did DOBBHOFF(R) RETRIEVAL FORCEPS receive FDA 510(k) clearance?

DOBBHOFF(R) RETRIEVAL FORCEPS received FDA 510(k) clearance on 1990-07-03, under 510(k) number K901744.

Who is the listed applicant for DOBBHOFF(R) RETRIEVAL FORCEPS?

The FDA 510(k) record lists Biosearch Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

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

The FDA product code for DOBBHOFF(R) RETRIEVAL FORCEPS is KQW.

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Other records listing Biosearch Medical Products, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K051480ENTERAL FEEDING TUBEK970145PERINEOMETER & VAGINAL PROBE (BIOFEEDBACK MONITOR #20 AND VAGINAL PROBE)K964871BIOSEARCH SYRING FLUSHING/CLEANING PUMP FOR BIOSEARCH ENDOSCOPIC INSTRUMENTSK951260URINARY INTERMITTENT CATHETERS W/O HYDROMER HYDROPHILIC LUBRICANTK944614MEGA-BRUSH, ENDOSCOPIC MASS CYTOLOGY - CELLUAR RETRIEVAL SYSTEMK932295NON-BALLOON REPLACEMENT GASTROSTOMY KIT

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Related Devices (Code: KQW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K926237O'BRIEN GONIOMETERSgarlato Laboratories, Inc.K870767THE (CROM) TESTERTwin City Surgical, Inc.K850082HAND HELD GONIOMETERChattanooga Group, Inc.K831550FINGER BONIOMETER BK7506Fred Sammons, Inc.K812778THE TELOS EQUIPMENTThe Telos Co.K810441UNIVERSAL GONIMETERFred Sammons, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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