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FDA 510(k)

RAZEL MODEL C

K-Number: K811272 · 1981-07-10

ApplicantRazel Scientific Instruments, Inc.
Decision Date1981-07-10
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RAZEL MODEL C is the device name listed in this FDA 510(k) record. The listed applicant is Razel Scientific Instruments, Inc.. It received FDA 510(k) clearance on 1981-07-10 under 510(k) number K811272. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RAZEL MODEL C?

RAZEL MODEL C is a medical device that received FDA 510(k) clearance on 1981-07-10. The listed applicant is Razel Scientific Instruments, Inc.. The 510(k) number is K811272.

When did RAZEL MODEL C receive FDA 510(k) clearance?

RAZEL MODEL C received FDA 510(k) clearance on 1981-07-10, under 510(k) number K811272.

Who is the listed applicant for RAZEL MODEL C?

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

What is the FDA product code for RAZEL MODEL C?

The FDA product code for RAZEL MODEL C is FRN.

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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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