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FDA 510(k)

CAST CUTTER/CAST SAW/INSTRUMENT

K-Number: K820351 · 1982-03-02

ApplicantBlack & Decker(Tm)
Decision Date1982-03-02
Product CodeLGH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CAST CUTTER/CAST SAW/INSTRUMENT is the device name listed in this FDA 510(k) record. The listed applicant is Black & Decker(Tm). It received FDA 510(k) clearance on 1982-03-02 under 510(k) number K820351. The device is classified under product code LGH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAST CUTTER/CAST SAW/INSTRUMENT?

CAST CUTTER/CAST SAW/INSTRUMENT is a medical device that received FDA 510(k) clearance on 1982-03-02. The listed applicant is Black & Decker(Tm). The 510(k) number is K820351.

When did CAST CUTTER/CAST SAW/INSTRUMENT receive FDA 510(k) clearance?

CAST CUTTER/CAST SAW/INSTRUMENT received FDA 510(k) clearance on 1982-03-02, under 510(k) number K820351.

Who is the listed applicant for CAST CUTTER/CAST SAW/INSTRUMENT?

The FDA 510(k) record lists Black & Decker(Tm) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CAST CUTTER/CAST SAW/INSTRUMENT?

The FDA product code for CAST CUTTER/CAST SAW/INSTRUMENT is LGH.

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Other records listing Black & Decker(Tm) 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.

K812438SAGITTAL SAWK812437150 DRIVER REAMERK812440POWER PACKK812436450/800 DRILLK812439DUAL MPC CHARGERK800314POWER PACK

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Related Devices (Code: LGH)

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.

K932653SWISSTEK 2000(TM) CAST REMOVAL SYSTEMCarapace, Inc.K901677CARAPACE PORTABLE CAST SAW, SWISS-EX CAST CUTTERBuckman Co., Inc.K893380QCR SYSTEM I AND QCR SYSTEM IIBremer Mfg. & Tool Co., Inc.K895861DELTA-TECH(TM) CAST REMOVAL SYSTEMJohnson & Johnson Professionals, Inc.K873723PLASTER VACUUM, 230V MODEL NO. 4183-161Martin MedicalK873721PLASTER VACUUM, 115V MODEL NO. 4183-160Martin Medical

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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