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FDA 510(k)

PODIATRIC MATERIAL

K-Number: K780391 · 1978-06-14

ApplicantCrown Delta Corp.
Decision Date1978-06-14
Product CodeMNE
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PODIATRIC MATERIAL is the device name listed in this FDA 510(k) record. The listed applicant is Crown Delta Corp.. It received FDA 510(k) clearance on 1978-06-14 under 510(k) number K780391. The device is classified under product code MNE. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PODIATRIC MATERIAL?

PODIATRIC MATERIAL is a medical device that received FDA 510(k) clearance on 1978-06-14. The listed applicant is Crown Delta Corp.. The 510(k) number is K780391.

When did PODIATRIC MATERIAL receive FDA 510(k) clearance?

PODIATRIC MATERIAL received FDA 510(k) clearance on 1978-06-14, under 510(k) number K780391.

Who is the listed applicant for PODIATRIC MATERIAL?

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

What is the FDA product code for PODIATRIC MATERIAL?

The FDA product code for PODIATRIC MATERIAL is MNE.

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Other records listing Crown Delta 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.

K122974TRYOUT-VPS HOLDING PASTEK041028CROWN DELTA HYDROPHILIC IMPRESSION MATERIALK955288HEARING AID IMPRESSION MATERIALK940132PODIATRIC MATERIALK930248VINYL POLYSILOXANE 2 COMPONENT VULCANIZING SYSTEMK926150VINYL ADDITION SILICONE SYSTEM

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Related Devices (Code: MNE)

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.

K940132PODIATRIC MATERIALCrown Delta 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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