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FDA 510(k)

MARKMAN TEMPLATE SYSTEM

K-Number: K970306 · 1997-11-20

ApplicantBarry Markman, M.D.
Decision Date1997-11-20
Product CodeGAH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MARKMAN TEMPLATE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Barry Markman, M.D.. It received FDA 510(k) clearance on 1997-11-20 under 510(k) number K970306. The device is classified under product code GAH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MARKMAN TEMPLATE SYSTEM?

MARKMAN TEMPLATE SYSTEM is a medical device that received FDA 510(k) clearance on 1997-11-20. The listed applicant is Barry Markman, M.D.. The 510(k) number is K970306.

When did MARKMAN TEMPLATE SYSTEM receive FDA 510(k) clearance?

MARKMAN TEMPLATE SYSTEM received FDA 510(k) clearance on 1997-11-20, under 510(k) number K970306.

Who is the listed applicant for MARKMAN TEMPLATE SYSTEM?

The FDA 510(k) record lists Barry Markman, M.D. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MARKMAN TEMPLATE SYSTEM?

The FDA product code for MARKMAN TEMPLATE SYSTEM is GAH.

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Related Devices (Code: GAH)

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

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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