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FDA 510(k)

PETITES BETWEEN-PERIOD PROTECTORS

K-Number: K771547 · 1977-09-20

Applicant3M Company
Decision Date1977-09-20
Product CodeHHL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

PETITES BETWEEN-PERIOD PROTECTORS is the device name listed in this FDA 510(k) record. The listed applicant is 3M Company. It received FDA 510(k) clearance on 1977-09-20 under 510(k) number K771547. The device is classified under product code HHL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PETITES BETWEEN-PERIOD PROTECTORS?

PETITES BETWEEN-PERIOD PROTECTORS is a medical device that received FDA 510(k) clearance on 1977-09-20. The listed applicant is 3M Company. The 510(k) number is K771547.

When did PETITES BETWEEN-PERIOD PROTECTORS receive FDA 510(k) clearance?

PETITES BETWEEN-PERIOD PROTECTORS received FDA 510(k) clearance on 1977-09-20, under 510(k) number K771547.

Who is the listed applicant for PETITES BETWEEN-PERIOD PROTECTORS?

The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PETITES BETWEEN-PERIOD PROTECTORS?

The FDA product code for PETITES BETWEEN-PERIOD PROTECTORS is HHL.

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 3M Company 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.

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Related Devices (Code: HHL)

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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