FDA 510(k)

EMBEDDING RINGS

K-Number: K831333 · 1983-05-25

ApplicantSurgipath Medical Industries, Inc.

Decision Date1983-05-25

Product CodeKER

Advisory CommitteePA

DecisionSubstantially Equivalent

Device Summary

EMBEDDING RINGS 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 1983-05-25 under 510(k) number K831333. 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 EMBEDDING RINGS?

EMBEDDING RINGS is a medical device that received FDA 510(k) clearance on 1983-05-25. The listed applicant is Surgipath Medical Industries, Inc.. The 510(k) number is K831333.

When did EMBEDDING RINGS receive FDA 510(k) clearance?

EMBEDDING RINGS received FDA 510(k) clearance on 1983-05-25, under 510(k) number K831333.

Who is the listed applicant for EMBEDDING RINGS?

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 EMBEDDING RINGS?

The FDA product code for EMBEDDING RINGS is KER.

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Other records listing Surgipath Medical Industries, Inc. as applicant

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Related Devices (Code: KER)

K831922EMBEDDING RINGPolymer Technology Corp.K831900MACLEAN-FOGG, DISP. BASE MOLDPolymer Technology Corp.K831335DISPOSABLE BASE MOLDSurgipath 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.