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FDA 510(k)

MONOJECT PULP-CAPPING MATERIAL

K-Number: K791088 · 1979-10-22

ApplicantSherwood Medical Co.
Decision Date1979-10-22
Product CodeEJK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MONOJECT PULP-CAPPING MATERIAL is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Co.. It received FDA 510(k) clearance on 1979-10-22 under 510(k) number K791088. The device is classified under product code EJK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MONOJECT PULP-CAPPING MATERIAL?

MONOJECT PULP-CAPPING MATERIAL is a medical device that received FDA 510(k) clearance on 1979-10-22. The listed applicant is Sherwood Medical Co.. The 510(k) number is K791088.

When did MONOJECT PULP-CAPPING MATERIAL receive FDA 510(k) clearance?

MONOJECT PULP-CAPPING MATERIAL received FDA 510(k) clearance on 1979-10-22, under 510(k) number K791088.

Who is the listed applicant for MONOJECT PULP-CAPPING MATERIAL?

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

What is the FDA product code for MONOJECT PULP-CAPPING MATERIAL?

The FDA product code for MONOJECT PULP-CAPPING MATERIAL is EJK.

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Other records listing Sherwood Medical Co. as applicant

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Related Devices (Code: EJK)

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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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