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FDA 510(k)

RULE, PUPILLARY

K-Number: K873440 · 1987-09-21

ApplicantAllegheny Plastics, Inc.
Decision Date1987-09-21
Product CodeHMM
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

RULE, PUPILLARY is the device name listed in this FDA 510(k) record. The listed applicant is Allegheny Plastics, Inc.. It received FDA 510(k) clearance on 1987-09-21 under 510(k) number K873440. The device is classified under product code HMM. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RULE, PUPILLARY?

RULE, PUPILLARY is a medical device that received FDA 510(k) clearance on 1987-09-21. The listed applicant is Allegheny Plastics, Inc.. The 510(k) number is K873440.

When did RULE, PUPILLARY receive FDA 510(k) clearance?

RULE, PUPILLARY received FDA 510(k) clearance on 1987-09-21, under 510(k) number K873440.

Who is the listed applicant for RULE, PUPILLARY?

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

What is the FDA product code for RULE, PUPILLARY?

The FDA product code for RULE, PUPILLARY is HMM.

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Related Devices (Code: HMM)

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.

K882575DISTOMETERHagg-Streit Service, Inc.

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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