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FDA 510(k)

MODELS 134, 135 & 136 TRANSFER CART/TABLE

K-Number: K844711 · 1985-03-05

ApplicantTri W-G, Inc.
Decision Date1985-03-05
Product CodeINK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MODELS 134, 135 & 136 TRANSFER CART/TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Tri W-G, Inc.. It received FDA 510(k) clearance on 1985-03-05 under 510(k) number K844711. The device is classified under product code INK. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODELS 134, 135 & 136 TRANSFER CART/TABLE?

MODELS 134, 135 & 136 TRANSFER CART/TABLE is a medical device that received FDA 510(k) clearance on 1985-03-05. The listed applicant is Tri W-G, Inc.. The 510(k) number is K844711.

When did MODELS 134, 135 & 136 TRANSFER CART/TABLE receive FDA 510(k) clearance?

MODELS 134, 135 & 136 TRANSFER CART/TABLE received FDA 510(k) clearance on 1985-03-05, under 510(k) number K844711.

Who is the listed applicant for MODELS 134, 135 & 136 TRANSFER CART/TABLE?

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

What is the FDA product code for MODELS 134, 135 & 136 TRANSFER CART/TABLE?

The FDA product code for MODELS 134, 135 & 136 TRANSFER CART/TABLE is INK.

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 Tri W-G, 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 35 devices →

Related Devices (Code: INK)

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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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