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FDA 510(k)

LEE-ALLOY DISPOSABLE CAPSULES

K-Number: K780966 · 1978-08-21

ApplicantLee Pharmaceuticals
Decision Date1978-08-21
Product CodeDZS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LEE-ALLOY DISPOSABLE CAPSULES is the device name listed in this FDA 510(k) record. The listed applicant is Lee Pharmaceuticals. It received FDA 510(k) clearance on 1978-08-21 under 510(k) number K780966. 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 LEE-ALLOY DISPOSABLE CAPSULES?

LEE-ALLOY DISPOSABLE CAPSULES is a medical device that received FDA 510(k) clearance on 1978-08-21. The listed applicant is Lee Pharmaceuticals. The 510(k) number is K780966.

When did LEE-ALLOY DISPOSABLE CAPSULES receive FDA 510(k) clearance?

LEE-ALLOY DISPOSABLE CAPSULES received FDA 510(k) clearance on 1978-08-21, under 510(k) number K780966.

Who is the listed applicant for LEE-ALLOY DISPOSABLE CAPSULES?

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 LEE-ALLOY DISPOSABLE CAPSULES?

The FDA product code for LEE-ALLOY DISPOSABLE CAPSULES 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.K781243MERCURY DISP. CAPSULELee 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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