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FDA 510(k)

RIGID ENDOSCOPE

K-Number: K911348 · 1991-06-21

ApplicantBruel & Kjaer
Decision Date1991-06-21
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RIGID ENDOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Bruel & Kjaer. It received FDA 510(k) clearance on 1991-06-21 under 510(k) number K911348. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RIGID ENDOSCOPE?

RIGID ENDOSCOPE is a medical device that received FDA 510(k) clearance on 1991-06-21. The listed applicant is Bruel & Kjaer. The 510(k) number is K911348.

When did RIGID ENDOSCOPE receive FDA 510(k) clearance?

RIGID ENDOSCOPE received FDA 510(k) clearance on 1991-06-21, under 510(k) number K911348.

Who is the listed applicant for RIGID ENDOSCOPE?

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

What is the FDA product code for RIGID ENDOSCOPE?

The FDA product code for RIGID ENDOSCOPE is LNH.

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Other records listing Bruel & Kjaer 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.

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Official Source

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