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FDA 510(k)

AUTOMATIC PATIENT CHAIR PM2000 & A

K-Number: K842359 · 1984-09-19

ApplicantPlanmeca USA, Inc.
Decision Date1984-09-19
Product Code
DecisionSubstantially Equivalent

Device Summary

AUTOMATIC PATIENT CHAIR PM2000 & A is the device name listed in this FDA 510(k) record. The listed applicant is Planmeca USA, Inc.. It received FDA 510(k) clearance on 1984-09-19 under 510(k) number K842359. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTOMATIC PATIENT CHAIR PM2000 & A?

AUTOMATIC PATIENT CHAIR PM2000 & A is a medical device that received FDA 510(k) clearance on 1984-09-19. The listed applicant is Planmeca USA, Inc.. The 510(k) number is K842359.

When did AUTOMATIC PATIENT CHAIR PM2000 & A receive FDA 510(k) clearance?

AUTOMATIC PATIENT CHAIR PM2000 & A received FDA 510(k) clearance on 1984-09-19, under 510(k) number K842359.

Who is the listed applicant for AUTOMATIC PATIENT CHAIR PM2000 & A?

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

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Other records listing Planmeca USA, 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.

K111361PLANMED NUANCE EXCELK081699PLANMECA SOVEREIGNK923534PM2002 PROLINEK923533ADMARKK923462DELIGHTK923461PM2002 PROLINE, PM2002 PROLINE EC

View all 13 devices →

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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