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FDA 510(k)

PAGE TURNER

K-Number: K770032 · 1977-01-12

ApplicantPossum, Inc.
Decision Date1977-01-12
Product CodeILP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PAGE TURNER is the device name listed in this FDA 510(k) record. The listed applicant is Possum, Inc.. It received FDA 510(k) clearance on 1977-01-12 under 510(k) number K770032. The device is classified under product code ILP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PAGE TURNER?

PAGE TURNER is a medical device that received FDA 510(k) clearance on 1977-01-12. The listed applicant is Possum, Inc.. The 510(k) number is K770032.

When did PAGE TURNER receive FDA 510(k) clearance?

PAGE TURNER received FDA 510(k) clearance on 1977-01-12, under 510(k) number K770032.

Who is the listed applicant for PAGE TURNER?

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

What is the FDA product code for PAGE TURNER?

The FDA product code for PAGE TURNER is ILP.

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 Possum, 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.

Related Devices (Code: ILP)

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

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