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FDA 510(k)

PORTA-SCALE

K-Number: K770847 · 1977-06-08

ApplicantSr Instruments, Inc.
Decision Date1977-06-08
Product CodeFRI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PORTA-SCALE is the device name listed in this FDA 510(k) record. The listed applicant is Sr Instruments, Inc.. It received FDA 510(k) clearance on 1977-06-08 under 510(k) number K770847. The device is classified under product code FRI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PORTA-SCALE?

PORTA-SCALE is a medical device that received FDA 510(k) clearance on 1977-06-08. The listed applicant is Sr Instruments, Inc.. The 510(k) number is K770847.

When did PORTA-SCALE receive FDA 510(k) clearance?

PORTA-SCALE received FDA 510(k) clearance on 1977-06-08, under 510(k) number K770847.

Who is the listed applicant for PORTA-SCALE?

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

What is the FDA product code for PORTA-SCALE?

The FDA product code for PORTA-SCALE is FRI.

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.

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Other records listing Sr Instruments, 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.

K770848DAILY-WEIGHT

Related Devices (Code: FRI)

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.

K790130SCALE, DIGITAL CHAIRAcme Medical Scale Co.K770848DAILY-WEIGHTSr Instruments, Inc.

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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