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FDA 510(k)

CLEAR BLUE ENDOSCOPIC LENS FOG RDUCTION SOLUTION & CLEANING KIT

K-Number: K944776 · 1994-11-01

Decision Date1994-11-01
Product CodeFEB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CLEAR BLUE ENDOSCOPIC LENS FOG RDUCTION SOLUTION & CLEANING KIT is the device name listed in this FDA 510(k) record. The listed applicant is Blue Planet Industries, Inc.. It received FDA 510(k) clearance on 1994-11-01 under 510(k) number K944776. The device is classified under product code FEB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLEAR BLUE ENDOSCOPIC LENS FOG RDUCTION SOLUTION & CLEANING KIT?

CLEAR BLUE ENDOSCOPIC LENS FOG RDUCTION SOLUTION & CLEANING KIT is a medical device that received FDA 510(k) clearance on 1994-11-01. The listed applicant is Blue Planet Industries, Inc.. The 510(k) number is K944776.

When did CLEAR BLUE ENDOSCOPIC LENS FOG RDUCTION SOLUTION & CLEANING KIT receive FDA 510(k) clearance?

CLEAR BLUE ENDOSCOPIC LENS FOG RDUCTION SOLUTION & CLEANING KIT received FDA 510(k) clearance on 1994-11-01, under 510(k) number K944776.

Who is the listed applicant for CLEAR BLUE ENDOSCOPIC LENS FOG RDUCTION SOLUTION & CLEANING KIT?

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

What is the FDA product code for CLEAR BLUE ENDOSCOPIC LENS FOG RDUCTION SOLUTION & CLEANING KIT?

The FDA product code for CLEAR BLUE ENDOSCOPIC LENS FOG RDUCTION SOLUTION & CLEANING KIT is FEB.

Related Clinical Trials

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.

Other records listing Blue Planet Industries, 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.

Related Devices (Code: FEB)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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