PEG 6,000
K-Number: K863103 · 1987-01-13
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Device Summary
Frequently Asked Questions
What is the PEG 6,000?
PEG 6,000 is a medical device that received FDA 510(k) clearance on 1987-01-13. The listed applicant is J. D. Assoc.. The 510(k) number is K863103.
When did PEG 6,000 receive FDA 510(k) clearance?
PEG 6,000 received FDA 510(k) clearance on 1987-01-13, under 510(k) number K863103.
Who is the listed applicant for PEG 6,000?
The FDA 510(k) record lists J. D. Assoc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PEG 6,000?
The FDA product code for PEG 6,000 is CHH.
Other records listing J. D. Assoc. 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.
Related Devices (Code: CHH)
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.
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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