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FDA 510(k)

PALMA

K-Number: K882639 · 1988-11-25

ApplicantKelso Imports
Decision Date1988-11-25
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PALMA is the device name listed in this FDA 510(k) record. The listed applicant is Kelso Imports. It received FDA 510(k) clearance on 1988-11-25 under 510(k) number K882639. The device is classified under product code KGO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PALMA?

PALMA is a medical device that received FDA 510(k) clearance on 1988-11-25. The listed applicant is Kelso Imports. The 510(k) number is K882639.

When did PALMA receive FDA 510(k) clearance?

PALMA received FDA 510(k) clearance on 1988-11-25, under 510(k) number K882639.

Who is the listed applicant for PALMA?

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

What is the FDA product code for PALMA?

The FDA product code for PALMA is KGO.

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Related Devices (Code: KGO)

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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