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FDA 510(k)

PULLEN POCKET SCOPE

K-Number: K802818 · 1981-04-17

ApplicantP.A. Research Corp.
Decision Date1981-04-17
Product CodeIBJ
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

PULLEN POCKET SCOPE is the device name listed in this FDA 510(k) record. The listed applicant is P.A. Research Corp.. It received FDA 510(k) clearance on 1981-04-17 under 510(k) number K802818. The device is classified under product code IBJ. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PULLEN POCKET SCOPE?

PULLEN POCKET SCOPE is a medical device that received FDA 510(k) clearance on 1981-04-17. The listed applicant is P.A. Research Corp.. The 510(k) number is K802818.

When did PULLEN POCKET SCOPE receive FDA 510(k) clearance?

PULLEN POCKET SCOPE received FDA 510(k) clearance on 1981-04-17, under 510(k) number K802818.

Who is the listed applicant for PULLEN POCKET SCOPE?

The FDA 510(k) record lists P.A. Research Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PULLEN POCKET SCOPE?

The FDA product code for PULLEN POCKET SCOPE is IBJ.

Related Clinical Trials

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Other records listing P.A. Research Corp. 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.

K892771PATIENT EXAMINATION GLOVES (POLY)

Related Devices (Code: IBJ)

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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