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FDA 510(k)

MERCURY DISP. CAPSULE

K-Number: K781243 · 1978-09-20

ApplicantLee Pharmaceuticals
Decision Date1978-09-20
Product CodeDZS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MERCURY DISP. CAPSULE is the device name listed in this FDA 510(k) record. The listed applicant is Lee Pharmaceuticals. It received FDA 510(k) clearance on 1978-09-20 under 510(k) number K781243. The device is classified under product code DZS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MERCURY DISP. CAPSULE?

MERCURY DISP. CAPSULE is a medical device that received FDA 510(k) clearance on 1978-09-20. The listed applicant is Lee Pharmaceuticals. The 510(k) number is K781243.

When did MERCURY DISP. CAPSULE receive FDA 510(k) clearance?

MERCURY DISP. CAPSULE received FDA 510(k) clearance on 1978-09-20, under 510(k) number K781243.

Who is the listed applicant for MERCURY DISP. CAPSULE?

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

What is the FDA product code for MERCURY DISP. CAPSULE?

The FDA product code for MERCURY DISP. CAPSULE is DZS.

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Other records listing Lee Pharmaceuticals 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.

K924378RESTOBOND 4K912256PRECISE(R) BETA QUARTZ GLASS-CERAMIC INSERTK900809LEE-FISCHER CERAMIC REINFORCED PLASTIC BRACKETSK894315RESTOBOND 3/DENTIN-ENAMEL BONDING AGENTK881903PROSTHODENT VLK873123LEE COMPOSITE INLAY SYSTEM

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Related Devices (Code: DZS)

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.

K822610PRECAPSULED DENTAL AMALGAMSyntex Dental Products, Inc.K802967DISPERSALLOY-DISPERSED PHASE ALLOY SELF-Johnson & Johnson Professionals, Inc.K780966LEE-ALLOY DISPOSABLE CAPSULESLee Pharmaceuticals

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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