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FDA 510(k)

INSTRUMENT DETERGENT CONCENTRATE

K-Number: K933149 · 1994-02-16

ApplicantNobelpharma USA, Inc.
Decision Date1994-02-16
Product CodeFLG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INSTRUMENT DETERGENT CONCENTRATE is the device name listed in this FDA 510(k) record. The listed applicant is Nobelpharma USA, Inc.. It received FDA 510(k) clearance on 1994-02-16 under 510(k) number K933149. The device is classified under product code FLG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSTRUMENT DETERGENT CONCENTRATE?

INSTRUMENT DETERGENT CONCENTRATE is a medical device that received FDA 510(k) clearance on 1994-02-16. The listed applicant is Nobelpharma USA, Inc.. The 510(k) number is K933149.

When did INSTRUMENT DETERGENT CONCENTRATE receive FDA 510(k) clearance?

INSTRUMENT DETERGENT CONCENTRATE received FDA 510(k) clearance on 1994-02-16, under 510(k) number K933149.

Who is the listed applicant for INSTRUMENT DETERGENT CONCENTRATE?

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

What is the FDA product code for INSTRUMENT DETERGENT CONCENTRATE?

The FDA product code for INSTRUMENT DETERGENT CONCENTRATE is FLG.

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Other records listing Nobelpharma USA, Inc. as applicant

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Related Devices (Code: FLG)

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.

K944950KLENZYMECalgon Corp.K944494ALSA-KLENZCalgon Vestal Div.K944033BILL EVANS-KLENZCalgon Vestal Div.K940263NPH-KLENZCalgon Corp.K941163MON-KLENZCalgon Vestal Div.K935063INSTRU KLENZCalgon Corp.

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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