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FDA 510(k)

CALIBRATED GRASPING TUBES

K-Number: K770148 · 1977-02-01

ApplicantMaddak, Inc.
Decision Date1977-02-01
Product CodeISD
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CALIBRATED GRASPING TUBES is the device name listed in this FDA 510(k) record. The listed applicant is Maddak, Inc.. It received FDA 510(k) clearance on 1977-02-01 under 510(k) number K770148. The device is classified under product code ISD. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CALIBRATED GRASPING TUBES?

CALIBRATED GRASPING TUBES is a medical device that received FDA 510(k) clearance on 1977-02-01. The listed applicant is Maddak, Inc.. The 510(k) number is K770148.

When did CALIBRATED GRASPING TUBES receive FDA 510(k) clearance?

CALIBRATED GRASPING TUBES received FDA 510(k) clearance on 1977-02-01, under 510(k) number K770148.

Who is the listed applicant for CALIBRATED GRASPING TUBES?

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

What is the FDA product code for CALIBRATED GRASPING TUBES?

The FDA product code for CALIBRATED GRASPING TUBES is ISD.

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 Maddak, 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 51 devices →

Related Devices (Code: ISD)

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.

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