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FDA 510(k)

PIK POCKET (IRRIGATING TIP)

K-Number: K863131 · 1986-08-26

Decision Date1986-08-26
Product CodeEFS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PIK POCKET (IRRIGATING TIP) is the device name listed in this FDA 510(k) record. The listed applicant is Teledyne, Inc.. It received FDA 510(k) clearance on 1986-08-26 under 510(k) number K863131. The device is classified under product code EFS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PIK POCKET (IRRIGATING TIP)?

PIK POCKET (IRRIGATING TIP) is a medical device that received FDA 510(k) clearance on 1986-08-26. The listed applicant is Teledyne, Inc.. The 510(k) number is K863131.

When did PIK POCKET (IRRIGATING TIP) receive FDA 510(k) clearance?

PIK POCKET (IRRIGATING TIP) received FDA 510(k) clearance on 1986-08-26, under 510(k) number K863131.

Who is the listed applicant for PIK POCKET (IRRIGATING TIP)?

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

What is the FDA product code for PIK POCKET (IRRIGATING TIP)?

The FDA product code for PIK POCKET (IRRIGATING TIP) is EFS.

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 Teledyne, Inc. 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 10 devices →

Related Devices (Code: EFS)

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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