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FDA 510(k)

PRESSURIZER, EXETER CEMENT

K-Number: K781792 · 1979-02-08

ApplicantHowmedica Corp.
Decision Date1979-02-08
Product CodeKIZ
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

PRESSURIZER, EXETER CEMENT is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1979-02-08 under 510(k) number K781792. The device is classified under product code KIZ. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRESSURIZER, EXETER CEMENT?

PRESSURIZER, EXETER CEMENT is a medical device that received FDA 510(k) clearance on 1979-02-08. The listed applicant is Howmedica Corp.. The 510(k) number is K781792.

When did PRESSURIZER, EXETER CEMENT receive FDA 510(k) clearance?

PRESSURIZER, EXETER CEMENT received FDA 510(k) clearance on 1979-02-08, under 510(k) number K781792.

Who is the listed applicant for PRESSURIZER, EXETER CEMENT?

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

What is the FDA product code for PRESSURIZER, EXETER CEMENT?

The FDA product code for PRESSURIZER, EXETER CEMENT is KIZ.

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Other records listing Howmedica Corp. 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.

K983528MICRO DYNAMIC MESHK983404TYPE 3 FEMORAL COMPONENTSK980926DURATION II ACETABULAR COMPONENTS-ETHYLENE OXIDE STERILIZATIONK980925DURATION II TIBIAL INSERTS-ETHYLENE OXIDE STERILIZATIONK980626DURATION II ACETABULAR COMPONENTS-GAS PLASMA STERILIZATIONK980632DURATION II TIBIAL INSERTS - GAS PLASMA STERILIZATION

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Related Devices (Code: KIZ)

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.

K890542MULTIWELL CULTURE PLATE INSERTSBd Becton Dickinson Vacutainer Systems PreanalyticK873891TISSUE CULTURE DISHESNunc, Inc.K871483TISSUE CULTURE/BACTERIOLOGICAL PETRI DISHESIsratech Marketing Corp.K854724CEKK-ADHESIVE MATRIX-MULTIPLE WELL PLATE CAM-PLATELifetrac, Inc.K853634CORNING CELL WELLS-MULTIPLE WELL PLATESCorning Medical & ScientificK821687REMOVAWELL TISSUE CULTURE PLATE W/LIDDynatech 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.

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