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FDA 510(k)

VIBRAMETER

K-Number: K843486 · 1984-12-24

ApplicantSomedic AB
Decision Date1984-12-24
Product CodeLLN
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

VIBRAMETER is the device name listed in this FDA 510(k) record. The listed applicant is Somedic AB. It received FDA 510(k) clearance on 1984-12-24 under 510(k) number K843486. The device is classified under product code LLN. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIBRAMETER?

VIBRAMETER is a medical device that received FDA 510(k) clearance on 1984-12-24. The listed applicant is Somedic AB. The 510(k) number is K843486.

When did VIBRAMETER receive FDA 510(k) clearance?

VIBRAMETER received FDA 510(k) clearance on 1984-12-24, under 510(k) number K843486.

Who is the listed applicant for VIBRAMETER?

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

What is the FDA product code for VIBRAMETER?

The FDA product code for VIBRAMETER is LLN.

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Related Devices (Code: LLN)

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.

K072882PAIN VISION, MODEL PS-2100Osachi Co., Ltd.K030829VPT METERXilas Medical, Inc.K010981GSA GENITO SENSORY ANALYZERMedoc Ltd. Advanced Medical SystemsK964622MEDI-DX 7000Neuro-Diagnostic Assoc.K964815AP-4000, AIR PULSE SENSORY STIMULATORPentax Precision Instrument Corp.K970180VSA 3000 VIBRATORYN SENSORY ANALYZEREare Consulting Service

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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