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FDA 510(k)

R&R ABSORBENT POINTS

K-Number: K781605 · 1978-10-10

Decision Date1978-10-10
Product CodeEKN
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

R&R ABSORBENT POINTS is the device name listed in this FDA 510(k) record. The listed applicant is Ransom and Randolph. It received FDA 510(k) clearance on 1978-10-10 under 510(k) number K781605. The device is classified under product code EKN. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the R&R ABSORBENT POINTS?

R&R ABSORBENT POINTS is a medical device that received FDA 510(k) clearance on 1978-10-10. The listed applicant is Ransom and Randolph. The 510(k) number is K781605.

When did R&R ABSORBENT POINTS receive FDA 510(k) clearance?

R&R ABSORBENT POINTS received FDA 510(k) clearance on 1978-10-10, under 510(k) number K781605.

Who is the listed applicant for R&R ABSORBENT POINTS?

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

What is the FDA product code for R&R ABSORBENT POINTS?

The FDA product code for R&R ABSORBENT POINTS is EKN.

Related Clinical Trials

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.

Other records listing Ransom and Randolph 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.

View all 7 devices →

Related Devices (Code: EKN)

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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