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FDA 510(k)

DAILY-WEIGHT

K-Number: K770848 · 1977-06-08

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

Device Summary

DAILY-WEIGHT 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 K770848. 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 DAILY-WEIGHT?

DAILY-WEIGHT 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 K770848.

When did DAILY-WEIGHT receive FDA 510(k) clearance?

DAILY-WEIGHT received FDA 510(k) clearance on 1977-06-08, under 510(k) number K770848.

Who is the listed applicant for DAILY-WEIGHT?

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 DAILY-WEIGHT?

The FDA product code for DAILY-WEIGHT 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.

K770847PORTA-SCALE

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.K770847PORTA-SCALESr 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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