FDA 510(k)

DISPOSABLE BASE MOLD

K-Number: K831335 · 1983-05-16

ApplicantSurgipath Medical Industries, Inc.

Decision Date1983-05-16

Product CodeKER

Advisory CommitteePA

DecisionSubstantially Equivalent

Device Summary

DISPOSABLE BASE MOLD is the device name listed in this FDA 510(k) record. The listed applicant is Surgipath Medical Industries, Inc.. It received FDA 510(k) clearance on 1983-05-16 under 510(k) number K831335. The device is classified under product code KER. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE BASE MOLD?

DISPOSABLE BASE MOLD is a medical device that received FDA 510(k) clearance on 1983-05-16. The listed applicant is Surgipath Medical Industries, Inc.. The 510(k) number is K831335.

When did DISPOSABLE BASE MOLD receive FDA 510(k) clearance?

DISPOSABLE BASE MOLD received FDA 510(k) clearance on 1983-05-16, under 510(k) number K831335.

Who is the listed applicant for DISPOSABLE BASE MOLD?

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

What is the FDA product code for DISPOSABLE BASE MOLD?

The FDA product code for DISPOSABLE BASE MOLD is KER.

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Other records listing Surgipath Medical Industries, Inc. as applicant

K883217SCHIFF REAGENT K881921C-E BRUSH K881922CYTOJARS PREFILLED WITH CYTOLOGY PRESERVATIVE K881659TISSUE SECTION ADHESIVE K863549REUSABLE/DISPOSABLE AUTOPSY KNIFE SET K863616KNIFE MAKER

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Related Devices (Code: KER)

K831922EMBEDDING RINGPolymer Technology Corp.K831900MACLEAN-FOGG, DISP. BASE MOLDPolymer Technology Corp.K831333EMBEDDING RINGSSurgipath Medical Industries, Inc.K772149LANCER BIOPSY HOLDERSherwood Medical Industries

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.