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FDA 510(k)

NK PRESSURE-SPECIFIED SENSORY DEVICE, MODEL PSSD-001

K-Number: K934368 · 1994-08-11

ApplicantNk Biotechnical Engineering Co.
Decision Date1994-08-11
Product CodeLLN
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NK PRESSURE-SPECIFIED SENSORY DEVICE, MODEL PSSD-001 is the device name listed in this FDA 510(k) record. The listed applicant is Nk Biotechnical Engineering Co.. It received FDA 510(k) clearance on 1994-08-11 under 510(k) number K934368. 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 NK PRESSURE-SPECIFIED SENSORY DEVICE, MODEL PSSD-001?

NK PRESSURE-SPECIFIED SENSORY DEVICE, MODEL PSSD-001 is a medical device that received FDA 510(k) clearance on 1994-08-11. The listed applicant is Nk Biotechnical Engineering Co.. The 510(k) number is K934368.

When did NK PRESSURE-SPECIFIED SENSORY DEVICE, MODEL PSSD-001 receive FDA 510(k) clearance?

NK PRESSURE-SPECIFIED SENSORY DEVICE, MODEL PSSD-001 received FDA 510(k) clearance on 1994-08-11, under 510(k) number K934368.

Who is the listed applicant for NK PRESSURE-SPECIFIED SENSORY DEVICE, MODEL PSSD-001?

The FDA 510(k) record lists Nk Biotechnical Engineering Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NK PRESSURE-SPECIFIED SENSORY DEVICE, MODEL PSSD-001?

The FDA product code for NK PRESSURE-SPECIFIED SENSORY DEVICE, MODEL PSSD-001 is LLN.

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Other records listing Nk Biotechnical Engineering Co. 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.

K923965NK GRASP SENSOR, MODEL GA002K923964NK GRASP SENSOR, MODEL GA001K923963NK DIGI-GRIP SENSOR, MODEL DGR001K921268NK DYNA-GRIP SENSOR, MODEL DG001K921266NK MEDICAL MICROMETER, MODEL MC001K914055PINCH SENSOR, MODEL PF001

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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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