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FDA 510(k)

SAF FIXATIVE

K-Number: K803054 · 1980-12-22

ApplicantRemel Co.
Decision Date1980-12-22
Product CodeIGB
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

SAF FIXATIVE is the device name listed in this FDA 510(k) record. The listed applicant is Remel Co.. It received FDA 510(k) clearance on 1980-12-22 under 510(k) number K803054. The device is classified under product code IGB. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAF FIXATIVE?

SAF FIXATIVE is a medical device that received FDA 510(k) clearance on 1980-12-22. The listed applicant is Remel Co.. The 510(k) number is K803054.

When did SAF FIXATIVE receive FDA 510(k) clearance?

SAF FIXATIVE received FDA 510(k) clearance on 1980-12-22, under 510(k) number K803054.

Who is the listed applicant for SAF FIXATIVE?

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

What is the FDA product code for SAF FIXATIVE?

The FDA product code for SAF FIXATIVE is IGB.

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.

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Other records listing Remel Co. 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.

K013711BACTI-SWAB DRYK965151A.C.T. IIIK965150A.C.T. IVK965152A.C.T. IIK965149A.C.T. IK960090CALCOFLUOR WHITE STAIN KIT

View all 137 devices →

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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