510(k) K780966
- Device
- LEE-ALLOY DISPOSABLE CAPSULES
- Applicant
- LEE PHARMACEUTICALS
- 510(k) number
- K780966
- Product code
- DZS
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1978-08-21
- Date received
- 1978-06-12
- Regulation
- 872.3110
- Classification name
- Capsule, Dental, Amalgam
- Medical specialty
- Dental
- Review panel
- Dental
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers#
- 3006153346
- 3008887731
- 3038718579
- 3012421607
- 3031564283
- 3012187973
- 3043648115
- 3008912871
- 2246990
- 3012312751
- 2020703
- 2024312
- 3009171220
- 8030067
- 3004140838
- 3005176727
- 2183301
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code DZS #
Legacy Summary#
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FDA Review#
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