FDA 510(k)

VASPAR SEALENT

K-Number: K812191 · 1981-08-31

Decision Date1981-08-31

Product CodeKEO

Advisory CommitteePA

DecisionSubstantially Equivalent

Device Summary

VASPAR SEALENT is the device name listed in this FDA 510(k) record. The listed applicant is American Scientific Products. It received FDA 510(k) clearance on 1981-08-31 under 510(k) number K812191. The device is classified under product code KEO. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VASPAR SEALENT?

VASPAR SEALENT is a medical device that received FDA 510(k) clearance on 1981-08-31. The listed applicant is American Scientific Products. The 510(k) number is K812191.

When did VASPAR SEALENT receive FDA 510(k) clearance?

VASPAR SEALENT received FDA 510(k) clearance on 1981-08-31, under 510(k) number K812191.

Who is the listed applicant for VASPAR SEALENT?

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

What is the FDA product code for VASPAR SEALENT?

The FDA product code for VASPAR SEALENT is KEO.

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Other records listing American Scientific Products as applicant

K864824INFECTIOUS TISSUE KIT K844042BLOOD DILUTION VIAL K831634GLUCOSE REAGENT B6360-11 K831625UREA NITROGEN-BUN-REAGENTS B6360-12 K831626UREA NITROGEN-BUN-REAGENTS B6370-11A K831628CREATININE REAGENTS B6370-13

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Related Devices (Code: KEO)

K893772TISSUE EMBEDDING MEDIUMStephens Scientific K862223MICRO THIN* PARAFFINRichard-Allan Medical Ind., Inc.K862141HISTOLOGY PARAFFINErie Scientific Co.K861270BLUE RIBBON PARAFFIN INFILTRATION/EMBEDDING MED.Surgipath Medical Industries, Inc.K842053PARAPLAST EXTRA TISSUE EMBEDDING MED.Sherwood Medical Co.K833071TECHNICON PARACUTTechnicon Instruments 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.