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FDA 510(k)

BILIBLANKET LIGHT METER

K-Number: K910571 · 1992-07-28

ApplicantOhmeda Medical
Decision Date1992-07-28
Product CodeLBI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BILIBLANKET LIGHT METER is the device name listed in this FDA 510(k) record. The listed applicant is Ohmeda Medical. It received FDA 510(k) clearance on 1992-07-28 under 510(k) number K910571. The device is classified under product code LBI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BILIBLANKET LIGHT METER?

BILIBLANKET LIGHT METER is a medical device that received FDA 510(k) clearance on 1992-07-28. The listed applicant is Ohmeda Medical. The 510(k) number is K910571.

When did BILIBLANKET LIGHT METER receive FDA 510(k) clearance?

BILIBLANKET LIGHT METER received FDA 510(k) clearance on 1992-07-28, under 510(k) number K910571.

Who is the listed applicant for BILIBLANKET LIGHT METER?

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

What is the FDA product code for BILIBLANKET LIGHT METER?

The FDA product code for BILIBLANKET LIGHT METER is LBI.

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Other records listing Ohmeda Medical 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.

K123309GIRAFFE AND PANDA WARMERSK101788GIRAFFE OMNIBEDK101778GIRAFFE INCUBATORK090697MODIFICATION TO: GIRAFFE AND PANDA WARMERK072157MODIFICATION TO GIRAFFE AND PANDA WARMERS (GIRAFFE AND PANDA UNINTERRUPTIBLE POWER SUPPLY)K070377GIRAFFE AND PANDA WARMER

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Related Devices (Code: LBI)

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

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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