Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

PTT 6200 ELEVATION THERAPY TABLE

K-Number: K953622 · 1995-09-11

Decision Date1995-09-11
Product CodeINQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PTT 6200 ELEVATION THERAPY TABLE is the device name listed in this FDA 510(k) record. The listed applicant is U.S. Table, Inc.. It received FDA 510(k) clearance on 1995-09-11 under 510(k) number K953622. The device is classified under product code INQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PTT 6200 ELEVATION THERAPY TABLE?

PTT 6200 ELEVATION THERAPY TABLE is a medical device that received FDA 510(k) clearance on 1995-09-11. The listed applicant is U.S. Table, Inc.. The 510(k) number is K953622.

When did PTT 6200 ELEVATION THERAPY TABLE receive FDA 510(k) clearance?

PTT 6200 ELEVATION THERAPY TABLE received FDA 510(k) clearance on 1995-09-11, under 510(k) number K953622.

Who is the listed applicant for PTT 6200 ELEVATION THERAPY TABLE?

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

What is the FDA product code for PTT 6200 ELEVATION THERAPY TABLE?

The FDA product code for PTT 6200 ELEVATION THERAPY TABLE is INQ.

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 U.S. Table, 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: INQ)

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.

↑