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FDA 510(k)

FAST FIND GRIND

K-Number: K934755 · 1993-11-19

ApplicantWebb Research Ii, Inc.
Decision Date1993-11-19
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FAST FIND GRIND is the device name listed in this FDA 510(k) record. The listed applicant is Webb Research Ii, Inc.. It received FDA 510(k) clearance on 1993-11-19 under 510(k) number K934755. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FAST FIND GRIND?

FAST FIND GRIND is a medical device that received FDA 510(k) clearance on 1993-11-19. The listed applicant is Webb Research Ii, Inc.. The 510(k) number is K934755.

When did FAST FIND GRIND receive FDA 510(k) clearance?

FAST FIND GRIND received FDA 510(k) clearance on 1993-11-19, under 510(k) number K934755.

Who is the listed applicant for FAST FIND GRIND?

The FDA 510(k) record lists Webb Research Ii, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FAST FIND GRIND?

The FDA product code for FAST FIND GRIND is KPR.

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Other records listing Webb Research Ii, 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.

K003773CLEAN SCRAPE

Related Devices (Code: KPR)

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.

K260227EXSYS DEXi (EXSYS DEXi-S40S); EXSYS DEXi (EXSYS DEXi-S40P); EXSYS DEXi (EXSYS DEXi-S40T); EXSYS DEXi (EXSYS DEXi-S50HDRTECH CorporationK260488MULTIX Impact; MULTIX Impact CSiemens Medical Solutions USA, Inc.K260481GC85ASamsung Electronics Co., Ltd.K260482DRE DuoJpi Healthcare Co, Ltd.K253446AeroDR TX c02Dk Medical Systems Co., Ltd.K250954DRX-Evolution Plus X-ray System, DRX-Compass Mobile X-ray System, Lux HD 35 detector, Lux HD 43 detectorCarestream Health

Official Source

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

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