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FDA 510(k)

P1808 MOBILE C-ARM IMAGE INTENSIFIER

K-Number: K827087 · 1982-03-04

ApplicantPrecise Optics
Decision Date1982-03-04
Product Code
DecisionSubstantially Equivalent

Device Summary

P1808 MOBILE C-ARM IMAGE INTENSIFIER is the device name listed in this FDA 510(k) record. The listed applicant is Precise Optics. It received FDA 510(k) clearance on 1982-03-04 under 510(k) number K827087. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the P1808 MOBILE C-ARM IMAGE INTENSIFIER?

P1808 MOBILE C-ARM IMAGE INTENSIFIER is a medical device that received FDA 510(k) clearance on 1982-03-04. The listed applicant is Precise Optics. The 510(k) number is K827087.

When did P1808 MOBILE C-ARM IMAGE INTENSIFIER receive FDA 510(k) clearance?

P1808 MOBILE C-ARM IMAGE INTENSIFIER received FDA 510(k) clearance on 1982-03-04, under 510(k) number K827087.

Who is the listed applicant for P1808 MOBILE C-ARM IMAGE INTENSIFIER?

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

Related Clinical Trials

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Other records listing Precise Optics 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.

K030061PS 3000 DIGATAL PHOTOSPOT SYSTEMK935580PHF20 20 MOBILE C-ARM IMAGE INTENSIFIERK932878PRECISION INTRA-ORAL SCOPESK914084ENDOSCOPESK914184P2020-8-0 BEAM-LIMITING DEVICEK911744PRECISION OPTICS CORPORATION LAPAROSCOPE

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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