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FDA 510(k)

ACCULATOR 487E

K-Number: K862352 · 1987-02-04

ApplicantAccu Science Corp.
Decision Date1987-02-04
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ACCULATOR 487E is the device name listed in this FDA 510(k) record. The listed applicant is Accu Science Corp.. It received FDA 510(k) clearance on 1987-02-04 under 510(k) number K862352. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCULATOR 487E?

ACCULATOR 487E is a medical device that received FDA 510(k) clearance on 1987-02-04. The listed applicant is Accu Science Corp.. The 510(k) number is K862352.

When did ACCULATOR 487E receive FDA 510(k) clearance?

ACCULATOR 487E received FDA 510(k) clearance on 1987-02-04, under 510(k) number K862352.

Who is the listed applicant for ACCULATOR 487E?

The FDA 510(k) record lists Accu Science Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACCULATOR 487E?

The FDA product code for ACCULATOR 487E is GZJ.

Related Clinical Trials

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.

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Other records listing Accu Science Corp. 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.

K871396ACCULATOR 287EP

Related Devices (Code: GZJ)

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.

K252712STIMPOD NMS460 Nerve StimulatorAlgiamed Technologies USA, Inc.K252767actiTENS miniSublimedK252236CP Relief Wand Rx - TENS/NMESN & C Holdings, LLCK232441Unipro (K-UNIPRO-US)Tenscare, Ltd.K241228TENSWaveZynex Medical OfficerK233046Electrical Neuromuscular Stimulator, Cure TrioOriental Inspiration Limited

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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